Synthesis of fluorene- and spirobifluorene-fused thiophenes

Article abstract of DOI:10.3987/COM-12-12427

A novel synthetic route to fluorene- and spirobifluorene-fused thiophenes is explored by starting with ninhydrin. The Diels-Alder cycloaddition was employed to construct the key intermediate, 2,3-bis(hydroxymethyl)-1,4-diphenyl- fluorenone, which was furt

Full text of DOI:10.3987/COM-12-12427

HETEROCYCLES, Vol. 85, No. 5, 2012
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HETEROCYCLES, Vol. 85, No. 5, 2012, pp. 1077 - 1088. © 2012 The Japan Institute of Heterocyclic Chemistry
Received, 15th January, 2012, Accepted, 12th March, 2012, Published online, 22nd March, 2012.
DOI: 10.3987/COM-12-12427
SYNTHESIS OF FLUORENE- AND SPIROBIFLUORENE-FUSED
THIOPHENES
Wen Yao, Qiancai Liu,* Yingbo Shi, and Jie Tang
Department of Chemistry, East China Normal University, Shanghai 200062,
China
* Corresponding author. Tel.: +86 21 6223 3490; fax: +86 21 6223 2414
E-mail: qcliu@chem.ecnu.edu.cn
Abstract – A novel synthetic route to fluorene- and spirobifluorene-fused
thiophenes is explored by starting with ninhydrin. The Diels-Alder cycloaddition
was
employed
to
construct
the
key
intermediate,
2,3-bis(hydroxymethyl)-1,4-diphenyl-fluorenone, which was further converted
stepwise to the target molecules. All of dihydrothiophenes and final products are
confirmed by 1H NMR, 13C NMR and mass spectrometry.
INTRODUCTION
Organic -conjugated oligomers and polymers are useful compounds as organic materials which are of
interests in the fields of organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs)
and organic solar cells. Heteroatom(s) are often contained or incorporated in the -conjugated systems,
and these heteroatom(s) play very important roles in the properties of the materials.1 Heteroatom(s)
cooperated polyaromatic hydrocarbons (PAHs) have attracted numerous attention due to their potentials
for device fabrication. In particular, fluorene and thiophene derivatives are notable structural motifs to
diverse PAHs for various applications in different materials.2a,2b For examples, linear- and angular-shaped
polyacene-fused thiophenes have been used in the areas of organic field-effect transistors and organic
photovoltaic devices.2c,2d Conventional multistep procedures are often employed for synthesis of
chacogen-incorporated derivatives with fluorene or spirofluorene rings, which have attracted considerable
attention recently in the field of organic optoelectronics, owing to their intriguing electronic properties.3
For example, thiophene-fused indeno-spirofluorenes have been reported as promising building blocks for

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HETEROCYCLES, Vol. 85, No. 5, 2012
the construction of optoelectronic materials in few cases.4 Compounds with spiro-sp3 carbon center have
become promising candidates for optoelectronic devices due to their high energy gap and low HOMO
levels.5 The above reasons led us to initiate our efforts on the study of fluorine-based thiophenes, which
are never studied in detail before and might be used as building blocks for further transformations. To our
best knowledge, only one example on fluorene-fused thiophene, 1,3-bis(4-bromophenyl)-9,9-dimethyl-
4,10-diphenyl-9H-fluoreno[2,3-c]thiophene, was reported so far by employing the Diels-Alder reaction of
cyclopentadienones with diaroylacetylenes and subsequently treated with P2O5 in the presence of base,6
and none of spirobifluorene-fused analogue has ever been reported.
As a part of our ongoing project on heteroatom-cooperated or containing fluorenes,7 we describe here the
latest progress on this type of compounds. The scope and synthetic applicability are quite versatile. The
results presented here afford an alternative route to fluorene-fused thiophenes, which should allow further
synthesis of a wide range of -conjugated fluorene- and spirobifluorene-based thiophenes by functional
transformation through either thienyl or fluorenyl subunit.
RESULTS AND DISCUSSION
For the preparation of fluorene-based thiophenes, 2,8-dioxo-1,3-diphenyl-2,8-dihydro-cyclopenta[a]-
indene (indanocyclone 1) was evaluated as building block because it has been revealed that 1 could act as
a promising precursor to construct substituted fluorenes. Compounds 1 could be easily accessible by the
reaction of nihydrin with 1,3-diphenylacetone under basic conditions by following literatures reported
before and its recent modification.8 We found that the Diels-Alder cycloaddition reaction between
indanocyclone and 1,4-Dihydroxy-2-butyne proceeded at 240 C in a short time (5 min) to afford
1,4-diphenyl-2,3-bis(hydroxymethyl)fluorenone (2) with an isolated yield of 43%. Then the two hydroxy
groups of 2 were protected by reacting with 2,2-dimethoxypropane (DMP) in the presence of p-TsOH in
THF to form 3 in excellent yield (85%), which was subsequently used in next steps. Compound 2 could
easily be converted into 9a (79%) in a refluxing mixture of 40% aq. HBr and chloroform in the presence
of Bu4NBr (TBAB). Compound 4 could be changed directly to compound 9b (78.6%) under condition
similar to that of 9a. For the indeno analogue, 3 was firstly converted into 4 by Wolff-Kishner reduction
(85%), followed by a halogen-alkali exchange to afford diethyl compound 5 (75.4%). For the
spirobifluorene-based analogue, the lithium salt formed in situ from 2-bromobiphenyl and BuLi was used
to react with 3 at -78 °C to form fluorenol 6 (86.5%), which was then converted into 7 (83%) under acidic
conditions (HCO2H/HCO2Na). Hydrolysis of 7 under basic condition resulted in compound 8. The
bromination of 5 and 8 was readily accomplished by similar procedure for preparation of 9a to form 9c
(80%) and 9d (90%).

HETEROCYCLES, Vol. 85, No. 5, 2012
1079
O
OH
OH
Ph
Ph
Ph
DMP/THF,
reflux
OH
O
O
240 °C
43%
+
Ph
85%
Ph
Br
Ph
O
HO
O
O
1
2
3
Ph
Br
Bu4NBr, aq.HBr
79%
Ph
O
Ph
9b
O
NH2NH2,KOH
180 °C, 85%
O
Br
Br
Ph
Ph
O
Ph
4
1. -78 °C,BuLi
2. EtBr
Bu4NBr, aq.HBr
80%
Ph
Ph
75%
5
9c
Br
Br
Ph
OH
OH
O
OCHO
OCHO
Ph
Ph
Ph
O
1.
Ph
Li
-78 °C
Ph
Bu4NBr, aq.HBr
90%
Ph
HCO H/HCO Na
Ph
KOH
88%
2
2
OH
74%
2. aq.NH4Cl
86.5%
6
7
9d
8
OH
OH
Br
Br
Ph
Ph
Bu4NBr, aq.HBr
79%
Ph
Ph
O
2
O
9a
Br
Br
Ph
Ph
Ph
R
R+R =O (a)
R =H (b)
R = Et (c)
S
S
Pd/C
-H2
Na2S
Ph
R R Ph
R+R = 2,2'-biphenyl (d)
Ph
R
R
R
9a
9b
10a (46%)
10b
11a (37%)
11b (40%)
(50%)
10c (55%)
11c
9c
9d
(46%)
11d (37%)
10d
(53%)
Scheme 1. Synthetic approach to the fluorene-fused thiophenes
With the four bis(bromomethyl)fluorene intermediates (9a-9d) in hands, our next step is to construct
2,5-dihydrothiophene ring. Generally 2,5-dihydrobenzo[b]isothiophene could easily be accomplished by

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HETEROCYCLES, Vol. 85, No. 5, 2012
the reaction of 1,2-di(bromomethyl)benzene with different sulfide sources (Na2S·9H2O or Na2SO3) in
polar solvents or by the reaction of elemental sulfur with reduction reagent such as SmI2.9,10 It was found
that steric congestions from substituents such as alkoxy and aryl groups at the either 3- or 3,6-positions
have no strong impact on the formation of 2,5-dihydrobenzoisothiophenes.11 All of the reactions could be
proceeded as expected. Then we decided to take use of Na2S·9H2O as a sulfide source, it was pleased to
find that all of the reactions could proceed smoothly to afford fluorene-based 2,5-dihydrothiophenes
(10a-10d) in isolated yields of 46% to 55%. Subsquently dehydrogenation of 2,5-dihydrothiophenes with
palladium on charcoal led to the formation of fluorene- and spirobifluorene-fused thiophenes (11a-11d,
yields from 37% to 46%).12,9a
The UV-Vis spectra of compounds 11a-11d (Figure 1) were measured with maximum absorptions at 307
nm (11a), 281nm (11b), 281nm (11c), 277 nm (11d) respectively, while fluorescence emission spectra
were obtained with blue emission at 442 nm (11b), 439 nm (11c), 437 nm (11d), however the maximum
emission of 11a appears at 515 nm, ca. 60 - 80 nm redshifted from those of 11b-11d (Figure 2), which
might be explained by the electron effect of fluorenyl carbonyl group in 11a.
0.9
0.8
11a
11b
0.7
11c
11d
0.6
0.5
0.4
0.3
0.2
0.1
0.0
-0.1
200
300
400
500
600
700
800
Wavelength(nm)
Figure1. The UV-Vis spectra of compounds 11a-11d

HETEROCYCLES, Vol. 85, No. 5, 2012
1081
1.0
0.8
0.6
0.4
0.2
0.0
11a
11b
11c
11d
350
400
450
500
550
Wavelength(nm)
Figure 2. The fluorescence emission spectra of 11a-11d
In conclusion, we have successfully completed novel fluorenyl and spirobifluorenyl-fused thiophenes,
which could be considered as precursors for blue emission materials from primary spectrometric study.
The key steps of the synthetic strategy involve the formation of 2,5-dihydrobenzoisothiophenes from
bis(bromomethyl)fluorene and spirobifluorene intermediates, and dehydrogenation of fluorene-based
2,5-dihydrothiophenes with palladium on charcoal.
EXPERIMENTAL
1. Instruments and materials
All manipulations for air- and moisture-sensitive operations are conducted by using of standard Schlenk
techniques. All chemicals are available from commercial sources and used without further purification.
Solvents are purified according to standard methods prior to use. Melting point was measured on an X-4
13
micrographic melting point apparatus. 1H NMR and C NMR spectra were measured on a Bruker DR ×
13
500 spectrometer (1H NMR 500 MHz, C NMR 125 Hz). Mass spectra were measured on micOTOF II
(ESI) spectrometer and Agilent 5973N mass spectrometer (EI).
2. Synthesis
1) 1,3-Diphenylindeno[a]cyclopenta-2,8-dione (indanocyclone 1) was synthesized by literature
method.8 To a solution of ninhydrin (4.86 g, 27.3 mmol) and 1,3-diphenyacetone (5.73 g, 27.3 mmol)

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HETEROCYCLES, Vol. 85, No. 5, 2012
dissolved in hot EtOH (40 mL) was added slowly as 10% KOH in MeOH (3.5 mL). The resulting
reaction mixture was heated at 75 C for 3 h with a color changed from yellow to deep red-brown. The
solid was filtered and recrystallized from toluene to afford 1 as red-brown crystals (7.43 g, 81.9%); mp
204-206 C (lit.,8a mp 204-206 C), 1H NMR (CDCl3, 500 MHz) δ: 8.61 (dd, J = 7.6 Hz, J = 1.0 Hz, 1H),
8.23-8.19 (m, 1H), 8.08-8.07 (m, 1H), 7.76-7.73 (m, 4H), 7.52-7.48 (m, 6H).
2) 1,4-Dipheny-2,3-bis(hydroxymethyl)-9-fluorenone (2)
The mixture of 1 (4 g, 12 mmol) and 1,4-dihydroxybutyne (1.3 g, 14.3 mmol) in a 50 mL round bottom
flask was heated at 240 C for 5 min, then it was cooled to room temperature and purified by column
chromatography (CH2Cl2 : EtOAc = 10 : 1), the resulting solid was washed with hexane to afford a yellow
powder (2 g, 43%); Rf = 0.11 (PE : EtOAc = 1 : 1); mp 224-225 C. 1H NMR (CDCl3, 500 MHz, ppm) δ:
7.57-7.51 (m, 3H), 7.48-7.42 (m, 4H), 7.40-7.38 (m, 2H), 7.32-7.30 (m, 2H), 7.11 (t, J = 7.5 Hz, 1H),
7.03 (td, J = 7.5 Hz, J = 1.0 Hz, 1H), 5.98 (d, J = 5.0 Hz, 1H), 4.56 (d, J = 5.0 Hz, 4H), 2.99 (br.s, 1H),
13
2.67 (br.s, 1H); C NMR (125 MHz, CDCl3, ppm) δ: 192.53, 145.16, 143.27, 142.29, 139.56, 187.82,
137.70, 136.18, 134.67, 134.17, 130.40, 129.22, 129.12, 128.79, 128.72, 128.36, 128.10, 127.82, 123.72,
123.14, 59.75, 59.30.
3) 3,3-Dimethyl-6,12-diphenyl-1H-fluoreno[3,2-e][1,3]dioxepin-11(5H)-one (3)
A mixture of 2 (11.26 g, 28.7 mmol), 2,2-dimethoxypropane (3.47 g, 34.4 mmol) and p-TsOH 2.6 g (14.4
mmol) in THF (200 mL) was heated to reflux for 4 h. Then the mixture was poured into aq. NaOH (20%,
200 mL) and extracted with CH2Cl2 (3 × 50 mL), the combined organic phase was dried over anhydrous
MgSO4. After workup, the residue was purified by column chromatography (PE : CH2Cl2 = 1 : 1) to form
1
a yellow solid (10.5 g, 85%); Rf = 0.26 (PE : CH2Cl2 = 1 : 1); mp 211-213 C. H NMR (CDCl3, 500
MHz, ppm) δ: 7.56-7.49 (m, 3H), 7.48-7.41 (m, 4H), 7.33-7.31 (m, 2H), 7.24-7.22 (m, 2H), 7.09 (t, J =
7.5 Hz, 1H), 7.03 (td, J = 7.5 Hz, J = 1.0 Hz, 1H), 5.93 (d, J = 5.0 Hz, 1H), 4.62 (d, J = 5.0 Hz, 4H), 1.39
13
(s, 6H); C NMR (125 MHz, CDCl3, ppm) δ: 192.59, 143.56, 143.33, 140.80, 138.95, 138.00, 137.59,
136.11, 135.05, 134.94, 133.94, 129.49, 129.34, 128.73, 128.41, 128.33, 128.31, 127.77, 123.63, 122.80,
120.13, 63.13, 62.25, 23.54.
4) 5,11-Dihydro-3,3-dimethyl-6,12-diphenyl-1H-fluoreno[3,2-e][1,3]dioxepine (4)
To a suspension of 3 (6.48 g, 15 mmol) in diethylene glycol (150 mL) was added hydrazine hydrate 13.5
mL (85%, 202 mmol), then the mixture was heated at 180 C and maintained for 2 h. After cooling to
room temperature, solid KOH (1.3 g, 22.5 mmol) was added, and it was again heated to 180 C till the
color turned to be white. The cooled mixture was poured into ice-cold water (200 mL) and extracted with
CH2Cl2 (3 × 50 mL), the organic phase was dried over MgSO4. After workup, the residue was
recrystallized from EtOH to afford a white solid (5.2 g, 83%), Rf = 0.25 (PE : CH2Cl2 = 2:1); mp 173-175
C. 1H NMR (CDCl3, 500 MHz, ppm) δ: 7.55-7.47 (m, 5H), 7.42 (t, J = 7.2 Hz, 1H), 7.34 (d, J = 7.0 Hz,
3H), 7.31 (d, J = 7.0 Hz, 2H), 7.11 (t, J = 7.2 Hz, 1H), 6.94 (t, J = 7.8 Hz, 1H), 6.22 (d, J = 7.6 Hz, 1H),

HETEROCYCLES, Vol. 85, No. 5, 2012
1083
4.73 (d, J = 9.0 Hz, 4H), 3.57 (s, 2H), 1.42 (s, 6H); 13C NMR (125 MHz, CDCl3, ppm) δ:143.99, 141.59,
141.06, 139.26, 139.19, 137.68, 136.52, 135.25, 134.25, 134.17, 129.18, 129.09, 128.87, 128.74, 127.69,
127.36, 126.24, 126.09, 124.52, 122.67, 102.01, 36.52, 23.73.
5) 1,4-Diphenyl-2,3-bis(bromomethyl)-9-fluorenone (9a)
To a solution of compound 2 (2.1 g, 5 mmol) in CHCl3 (50 mL) were added Bu4NBr (0.6 g, 2 mmol), aq.
HBr (40%, 10 mL) and conc. H2SO4 (1 mL), and the mixture was heated at 60 C for 72 h and poured
into water (200 mL). It was then extracted with CH2Cl2 (3 × 50 mL) and the organic phase was dried over
MgSO4. After workup, the crude product was isolated by column chromatography (CH2Cl2 : PE = 1 : 1)
to get a yellow solid (2.2 g, 79%), Rf = 0.68 (CH2Cl2 : PE = 2 : 3); mp 191-193 C. 1H NMR (CDCl3, 500
MHz, ppm) δ: 7.62-7.61 (m, 3H), 7.55-7.53 (m, 3H), 7.50-7.47 (m, 3H), 7.42-7.40 (m, 2H), 7.15 (t, J =
7.5 Hz, 1H), 7.09 (t, J = 7.5 Hz, 1H), 5.95 (d, J = 7.5 Hz, 1H), 4.52 (s, 4H); 13C NMR (125 MHz, CDCl3,
ppm) δ:191.96, 143.22, 142.86, 142.12, 141.83, 138.20, 136.90, 136.57, 135.19, 134.59,134.36, 131.16,
129.36, 129.13, 128.98, 128.86, 128.52, 128.23, 123.91, 123.28, 27.49, 27.19.
6) 9-Oxo-4,10-diphenylfluoreno[2,3-c]-2,5-dihydrothiophene (10a)
A mixture of Na2S·9H2O (1.5 g, 6.2 mmol) and THF solution in EtOH (VTHF : VEtOH = 1 : 5, 36 mL) in a
three-necked flask was heated to reflux under nitrogen, then a solution of 9a (2 g, 3.86 mmol) in THF (20
mL) was added slowly and the heating was continued for 3 h. It was stirred at room temperature overnight
before being poured into water and extracted with CH2Cl2. The organic phase was dried over MgSO4.
After workup, the crude product was purified by column chromatography (CH2Cl2 : PE = 3 : 2) to obtain
a yellow solid (0.7 g, 46%); Rf = 0.59 (CH2Cl2 : PE = 3 : 2); mp 270-272 C. 1H NMR (CDCl3, 500 MHz,
ppm) δ: 7.58-7.53 (m, 3H), 7.50-7.44 (m, 4H), 7.40-7.38 (m, 2H), 7.34-7.32 (m, 2H), 7.15-7.08 (m, 2H),
6.24 (d, J = 7.3 Hz, 1H), 4.04-4.00 (m, 4H); 13C NMR (125 MHz, CDCl3, ppm) δ: 192.14, 146.59, 143.05,
141.67, 141.03, 137.68, 137.44, 136.22, 135.06, 133.91, 133.63, 130.21, 129.21, 128.40, 128.28, 128.24,
128.08, 127.82, 123.64, 122.60, 37.85, 37.30. MS (EI): m/z = 390 [M+].
7) 9-Oxo-4,10-diphenylfluoreno[2,3-c]thiophene (11a)
A 100 mL three-necked round bottom flask were charged with 10a (0.7 g, 1.80 mmol); wet Pd/C (10%)
0.5 g (containing ca. 30% water) and xylenes (20 mL) and the mixture was heated to reflux for 48 h under
nitrogen. After completion, the mixture was filtered through a kieselguhr pad, the filtrate was evaporated
and the crude product was purified by column chromatography (CH2Cl2 : PE = 1 : 1) to afford a light
yellow solid (0.26 g, 37%); Rf = 0.50 (PE : CH2Cl2 = 2 : 3); mp 265-267 C. 1H NMR (CDCl3, 500 MHz,
ppm) δ: 7.65-7.53 (m, 12H), 7.22-7.20 (m, 3H), 6.61 (d, J = 6.5 Hz, 1H); 13C NMR (125 MHz, CDCl3,
ppm) δ: 191.67, 143.99, 141.62, 139.65, 137.75, 137.60, 137.03, 135.61, 134.13, 132.02, 129.31, 129.29,
128.42, 128.38, 128.09, 127.35, 124.73, 123.78, 123.65, 119.59. MS (EI): m/z = 388 [M+].
8) 1,4-Diphenyl-2,3-bis(bromomethyl)-9-fluorene (9b)
9b was prepared essentially the same procedure for 9a by employing 4 (1.9 g, 4.5 mmol), CHCl3 (50 mL),

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HETEROCYCLES, Vol. 85, No. 5, 2012
Bu4NBr (0.6 g, 2 mmol), aq. HBr (10 mL, 40%) and conc. H2SO4 (0.8 mL), and it was isolated (PE :
CH2Cl2 = 3 : 1) as a white solid (1.8 g, 78.6%); Rf = 0.65 (PE : CH2Cl2 = 3 : 1); mp 180-182 C. 1H NMR
(CDCl3, 500 MHz, ppm) δ: 7.62-7.55 (m, 5H), 7.50-7.49 (m, 5H), 7.37 (d, J = 7.5 Hz, 1H), 7.17 (t, J =
7.4 Hz, 1H), 6.98 (t, J = 7.6 Hz, 1H), 6.22 (d, J = 7.9 Hz, 1H), 4.68 (s, 4H), 3.63 (s, 2H); 13C NMR (125
MHz, CDCl3, ppm) δ: 144.03, 143.81, 140.97, 140.41, 140.11, 138.27, 138.04, 137.82, 134.49, 132.89,
129.21, 129.08, 128.90, 128.70, 128.26, 127.92, 126.91, 126.52, 124.56, 123.14, 37.17, 29.52, 28.87.
9) 4,10-Diphenylfluoreno[2,3-c]-2,5-dihydrothiophene (10b)
10b was prepared essentially the same as for 10a by employing Na2S·9H2O (0.3 g, 1.2 mmol), THF in
EtOH (18 mL), 10a (0.4 g, 0.8 mmol) in THF (20 mL), and purified (PE : CH2Cl2 = 3 : 1) as a white solid
1
(0.15 g, 50%); Rf = 0.48 (PE : CH2Cl2 = 4 : 1); mp 163-165 C. H NMR (CDCl3, 500 MHz, ppm) δ:
7.56-7.53 (m, 2H), 7.51-7.48 (m, 3H), 7.44-7.39 (m, 6H), 7.15 (t, J = 7.2 Hz, 1H), 6.99 (t, J = 7.5 Hz, 1H),
13
6.51 (d, J = 7.9 Hz, 1H), 4.16 (s, 2H), 4.07 (s, 2H), 3.71 (s, 2H); C NMR (125 MHz, CDCl3, ppm) δ:
144.17, 141.79, 141.24, 139.41, 139.16, 138.56, 137.36, 134.94, 132.98, 129.10, 128.71, 128.53, 127.80,
127.53, 126.31, 126.27, 124.67, 122.64, 37.77, 37.72, 36.07. MS (EI): m/z = 376 [M+].
10) 4,10-Diphenyl-9H-fluoreno[2,3-c]thiophene (11b)
11b was prepared essentially the same as for 11a by employing 10b (0.15 g, 0.4 mmol); wet Pd/C (10%)
0.06 g and xylenes (15 mL), and it was isolated (CH2Cl2 : PE = 5 : 1) as a solid (0.06 g, 40%); Rf = 0.68
(PE : CH2Cl2 = 4 : 1); mp 165-167 C. 1H NMR (CDCl3, 500 MHz, ppm) δ: 7.62-7.59 (m, 4H), 7.57-7.54
(m, 5H), 7.48-7.46 (m, 1H), 7.43-7.42 (m, 1H), 7.37 (d, J = 7.5 Hz, 1H), 7.28-7.27 (m, 1H), 7.18 (t, J =
7.5 Hz, 1H), 7.01 (t, J = 7.7 Hz, 1H), 6.71 (d, J = 7.9 Hz, 1H), 3.94 (s, 2H); 13C NMR (125 MHz, CDCl3,
ppm) δ: 144.31, 140.75, 138.96, 129.63, 129.29, 129.08, 128.68, 127.82, 127.47, 127.16, 126.41, 124.85,
123.64, 117.05, 115.09, 30.89. MS (EI): m/z = 374 [M+].
11) 11,11-Diethyl-5,11-dihydro-3,3-dimethyl-6,12-diphenyl-1H-fluoreno[3,2-e][1,3]dioxepine (5)
To a solution of 4 (2.22 g, 5.3 mmol) in THF (50 mL) at -78 C under nitrogen was added BuLi (3.2 mL,
2.5 M, 7.9 mmol) and the stirring continued for 30 min, then ethyl bromide (0.63 mL, 7.9 mmol) was
added. After addition, the mixture was allowed to warm to room temperature and stirred for 1 h. The
above procedure was exactly repeated once and then the reaction was quenched with saturated aq. NH4Cl
and extracted with CH2Cl2 (3 × 50 mL). After workup, the crude product was purified by column
chromatography (PE : CH2Cl2 = 3 : 1) and further washed with EtOH to afford 5 as a white solid (1.9 g,
75.4%), Rf = 0.33 (PE : CH2Cl2 = 2 : 1); mp 181-182 C. 1H NMR (CDCl3, 500 MHz, ppm) δ: 7.54-7.49
(m, 3H), 7.46-7.42 (m, 3H), 7.33 (d, J = 7. 0Hz, 2H), 7.28 (d, J = 6.5 Hz, 2H), 7.11 (t, J = 7.0 Hz, 2H),
6.87-6.85 (m, 1H), 6.05 (d, J = 8.0 Hz, 1H), 4.68 (s, 2H), 4.51 (s, 2H), 1.63 (q, J = 7.0 Hz, 4H), 1.39 (s,
13
6H), 0.25 (t, J = 7.0 Hz, 6H); C NMR (125 MHz, CDCl3, ppm) δ: 151.12, 143.25, 141.01, 139.46,
138.64, 138.44, 136.36, 135.12, 135.00, 134.33, 129.21, 129.17, 129.09, 128.13, 127.62, 127.47, 126.56,
126.09, 122.24, 121.43, 101.90, 63.08, 62.86, 57.43, 31.90, 23.66, 8.27.

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12) 1,4-Diphenyl-2,3-bis(bromomethyl)-9,9-diethylfluorene (9c)
9c was prepared essentially the same as 9a by employing 5 (1.9 g, 4.0 mmol), CHCl3 (50 mL), Bu4NBr
(0.68 g , 2.25 mmol), aq. HBr (40%, 12.5 mL) and conc. H2SO4 (1 mL), and it was purified (PE : CH2Cl2
= 4：1) as a white solid (1.8 g, 80%); Rf = 0.65 (PE : CH2Cl2 = 3 : 1); mp 181-183 C. 1H NMR (CDCl3,
500 MHz, ppm) δ: 7.56-7.48(m, 8H), 7.48-7.40 (m, 2H), 7.18-7.13 (m, 2H), 6.90 (t, J = 7.0 Hz, 1H), 6.05
(d, J = 8.0 Hz, 1H), 4.60 (s, 2H), 4.49 (s, 2H), 1.67-1.63 (m, 4H), 0.25 (t, J = 7.0 Hz, 6H); 13C NMR (125
MHz, CDCl3, ppm) δ: 151.20, 146.23, 141.23, 140.29, 139.83, 138.19, 137.59, 137.04, 134.34, 133.99,
129.36, 128.97, 128.12, 128.00, 127.78, 127.34, 126.35, 122.74, 121.50, 57.91, 31.76, 29.36, 28.88, 8.28.
13) 4,10-Diphenyl-9,9-diethylfluoreno[2,3-c]-2,5-dihyrothiophene (10c)
This is prepared similar to 10a by using of Na2S·9H2O (1.2 g, 4.8 mmol), THF in EtOH (24 mL) and 9c
(1.8 g, 3.2 mmol) in THF (10 mL) and, It was purified (CH2Cl2 : PE = 1 : 3) as a white solid (0.76 g,
55%), Rf = 0.63 (PE : CH2Cl2 = 4 : 1), mp 131-133 C. 1H NMR (CDCl3, 500 MHz，ppm) δ: 7.55-7.48 (m,
3H), 7.46-7.43 (m, 3H), 7.40-7.39 (m, 2H),7.32-7.30 (m, 2H), 7.16-7.15 (m, 2H), 6.94-6.91 (m, 1H), 6.36
13
(d, J = 7.9 Hz, 1H), 4.05 (s, 2H), 3.90 (s, 2H), 1.72 (q, J = 7.3 Hz , 4H), 0.30 (t, J = 7.7 Hz , 6H); C
NMR (125 MHz, CDCl3, ppm) δ: 151.17, 144.57, 140.77, 139.71, 139.27, 139.20, 138.69, 138.41, 135.14,
132.85, 129.05, 128.78, 128.47, 128.18, 127.69, 127.51, 126.69, 126.17, 122.18, 121.65, 57.10, 38.28,
37.95, 32.03, 8.33. MS (EI): m/z = 403 [M-CH2CH3]+
14) 4,10-Diphenyl-9,9-diethylfluoreno[2,3-c]thiophene (11c)
This is prepared similar to 11a by employing 10c (0.6 g, 1.38 mmol); wet Pd/C (10%) 0.2 g and xylenes
(15 mL). It was purified (CH2Cl2 : PE = 1 : 5) as a solid (0.27 g, 46%); Rf = 0.79 (PE : CH2Cl2 = 4 : 1);
mp 133-135 C. 1H NMR (CDCl3, 500 MHz, ppm) δ: 7.61-7.58 (m, 2H), 7.55-7.47 (m, 6H), 7.45-7.43 (m,
2H),7.21-7.14 (m, 3H), 6.96-6.92 (m, 2H), 6.58 (d, J = 7.9 Hz, 1H), 1.82-1.76 (m, 2H), 1.75-1.70 (m, 2H),
13
0.42 (t, J = 7.3 Hz, 6H); C NMR (125 MHz, CDCl3, ppm) δ: 151.16, 141.06, 140.74, 140.31, 139.21,
136.16, 129.72, 129.63, 129.40, 129.09, 127.99, 127.74, 127.54, 127.46, 126.32, 123.08, 122.00, 116.46,
56.19, 33.19, 8.64. MS (EI): m/z = 401 [M-CH2CH3]+.
15) 11-Hydroxyl-11-(2’-biphenyl)-5,11-dihydro-3,3-dimethyl-6,12-diphenyl-1H-fluoreno[3,2-e][1,3]-
dioxepine (6)
Under nitrogen, to a solution of 2-bromobiphenyl (2 g, 8.6 mmol) in THF (15 mL) cooled to -78 °C was
added dropwise BuLi (3.44 mL, 2.5 M in hexane, 8.6 mmol). Then a solution of 3 (2.3 g, 5.75 mmol) in
THF (15 mL) was added slowly and the mixture was kept for 1 h and warmed gradually to room
temperature, and the stirring was continued for another 1 h at room temperature and the reaction was
quenched with saturated aq. NH4Cl (50 mL). The mixture was extracted with CH2Cl2 (3 × 20 mL), the
organic phase was dried over MgSO4. After filtered, the filtration was evaporated and the residue was
subjected to column chromatography (PE : CH2Cl2 = 1 : 1), the product was further washed with hexane
to afford 6 (2.7 g, 86.5%); Rf = 0.15 (PE : CH2Cl2 = 1 : 2), mp 257-259 C. 1H NMR (CDCl3, 500 MHz,

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ppm) δ: 7.45-7.43 (m, 1H), 7.41-7.28 (m, 3H), 7.30 (d, J = 8.0 Hz, 1H), 7.27 (d, J = 7.0 Hz , 1H), 7.23 (t,
J = 7.0 Hz, 1H), 7.17-7.13 (m, 2H), 7.10 (t, J = 7.5 Hz, 1H), 7.02-6.97 (m, 5H), 6.88 (d, J = 7.0 Hz, 1H),
6.77 (d, J = 6.5Hz, 2H), 6.52-6.49 (m, 3H), 5.83 (s, 1H), 5.60 (d, J = 8.0 Hz, 1H), 4.63-4.43 (m, 4H), 2.34
(s, 1H), 1.41 (s, 3H), 1.36 (s, 3H); 13C NMR (125 MHz, CDCl3, ppm) δ: 151.21, 145.87, 141.00, 137.34,
136.63, 130.90, 129.13, 129.05, 128.67, 128.57, 128.13, 127.90, 127.84, 127.64, 127.37, 126.89, 126.73,
125.96, 125.70, 125.40, 123.95, 122.94, 101.92, 82.14, 62.81, 62.78, 23.85, 23.63.
16) 1,4-Diphenyl-2,3-bis(dimethylene formate)-9,9’-spirobifluorene (7)
A suspension of 6 (2.7 g, 4.6 mmol) and HCO2Na (1.75 g, 25 mmol) in HCO2H (150 mL) was refluxed
for 24 h before being poured into ice-water (500 mL). It was then extracted with CH2Cl2 (3 × 50 mL) and
washed with water to neutral, the organic phase was dried over MgSO4. After workup, the residue was
recrystallized from EtOH to afford a white solid (2 g, 74%); Rf = 0.25 (PE : CH2Cl2 = 1 : 2); mp 150-152
C. 1H NMR (CDCl3, 500 MHz, ppm) δ: 7.98 (s, 1H), 7.79 (s, 1H), 6.64-6.59 (m, 3H), 7.53 (d, J = 7.5 Hz,
2H), 7.32 (d, J = 7.5 Hz, 2H), 7.20 (t, J = 7.2 Hz, 2H), 7.07 (t, J = 7.5 Hz, 2H), 6.95-6.93 (m, 2H), 6.88 (t,
J = 7.5 Hz, 1H), 6.79 (d, J = 7.5 Hz, 2H), 6.62 (t, J = 7.8 Hz, 2H), 6.49-6.47 (m, 1H), 6.27-6.26 (m, 1H),
6.07 (d, J = 7.0 Hz, 2H), 5.15 (s, 2H), 4.85 (s, 2H); 13C NMR (125 MHz, CDCl3, ppm) δ: 178.04, 160.14,
159.99, 149.98, 147.60, 147.45, 142.06, 141.66, 140.23, 138.46, 138.07, 134.58, 132.86, 132.38, 129.43,
129.13, 128.78, 128.37, 128.04, 127.28, 127.21, 127.17, 126.60, 125.95, 123.63, 123.52, 123.29, 119.90,
65.64, 60.35, 60.32.
17) 1,4-Diphenyl-2,3-bis(hydroxymethyl)-9,9’-spirobifluorene (8)
To a solution of 7 (2 g, 3.45 mmol) in THF (50 mL) was added aq. KOH (10%, 10 mL), the mixture was
stirred for 30 min and poured into water. It was then extracted with CH2Cl2 (3 × 50 mL) and the organic
phase was washed with water for three times before subjected to be dried over MgSO4. After workup, the
residue was recrystallized from hexane to afford a white powder (1.6 g, 88%), Rf = 0.45 (PE : EtOAc = 1 :
1
1); mp 279-280 C. H NMR (CDCl3, 500 MHz, ppm) δ: 7.64-7.55 (m, 5H), 7.44 (d, J = 5.0 Hz, 2H),
7.20 (t, J = 7.5 Hz, 2H), 7.06 (t, J = 7.3 Hz, 2H), 6.92-6.82 (m, 3H), 6.79 (d, J = 7.5 Hz, 2H), 6.64 (t, J =
7.5 Hz, 2H), 6.47 (d, J = 7.0 Hz, 1H), 6.28 (d, J = 7.0 Hz, 1H) 6.10 (d, J = 7.5 Hz, 2H), 4.64 (s, 2H), 4.35
13
(s, 2H), 2.97 (br.s, 1H), 2.45 (br.s, 1H); C NMR (125 MHz, CDCl3, ppm) δ: 149.91, 148.06, 145.84,
142.03, 140.82, 139.99, 139.11, 138.32, 137.14, 135.75, 129.57, 129.05, 128.82, 127.94, 127.52, 127.16,
127.12, 127.01, 126.61, 125.59, 123.69, 123.40, 123.10, 119.81, 107.95, 65.64, 59.99, 59.91.
18) 1,4-Diphenyl-2,3-bis(bromomethyl)-9,9’-spirobifluorene (9d)
This is prepared essentially similar to 9a by employing 8 (1.6 g, 3.0 mmol), CHCl3 (50 mL), Bu4NBr (0.6
g, 2 mmol), aq. HBr (40%, 8 mL) and conc. H2SO4 (0.6 mL), and it was isolated (CH2Cl2 : PE = 1 : 3) as a
1
white solid (1.8 g, 90%), Rf = 0.75 (CH2Cl2 : PE = 1 : 3 ); mp 145-148 C. H NMR (CDCl3, 500 MHz,
ppm) δ: 7.69-7.62 (m, 5H), 7.33 (d, J = 7.5 Hz, 2H), 7.21 (t, J = 7.5 Hz, 2H), 7.09 (t, J = 7.4 Hz, 2H),
6.94-6.91 (m, 3H), 6.81 (d, J = 7.5 Hz, 2H), 6.68 (t, J = 7.5 Hz, 2H), 6.48-6.46 (m, 1H), 6.23-6.20 (m,

HETEROCYCLES, Vol. 85, No. 5, 2012
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13
1H), 6.17 (d, J = 7.1 Hz, 2H), 4.65 (s, 2H), 4.37 (s, 2H); C NMR (125 MHz, CDCl3, ppm) δ: 159.96,
147.65, 142.02, 140.96, 140.28, 137.93, 135.25, 134.72, 134.40, 129.41, 129.13, 128.84, 128.40, 127.94,
127.25, 127.23, 127.16, 126.58, 125.97, 123.71, 123.47, 123.19, 119.85, 109.65, 65.61, 28.86, 28.65.
19) 4,10-Diphenyl-9,9’-spirobifluoreno[2,3-c]-2,5-dihydrothiophene (10d)
This is prepared essentially similar to 10a by employing Na2S·9H2O (0.75g, 6.2 mmol), THF in EtOH (24
mL) and 9d (1.4 g, 2.1 mmol) in THF (10 mL). It was purified (CH2Cl2 : PE = 1 : 4) as a white solid (0.6
g, 53%); Rf = 0.46 (CH2Cl2 : PE = 1 : 4); mp 269-271 C. 1H NMR (CDCl3, 500 MHz, ppm) δ: 7.63-7.60
(m, 2H), 7.57-7.55 (m, 3H), 7.32 (d, J = 7.5 Hz, 2H), 7.20 (t, J = 7.4 Hz, 2H), 7.08 (t, J = 7.4 Hz, 2H),
6.97-6.87 (m, 3H), 6.83 (d, J = 7.5 Hz, 2H), 6.67 (t, J = 7.5 Hz, 2H), 6.52 (q, J = 7.5 Hz, 2H), 6.08 (d, J =
13
7.5 Hz, 2H), 4.09 (s, 2H), 3.77 (s, 2H); C NMR (125 MHz, CDCl3, ppm) δ: 149.90, 148.38, 145.43,
142.02, 140.75, 139.62, 139.37, 139.22, 136.36, 132.90, 129.18, 128.85, 128.00, 127.96, 127.32, 127.19,
127.15, 127.02, 126.91, 125.69, 123.71, 123.60, 122.67, 119.77, 37.87. MS (EI): m/z = 526 [M+].
20) 4,10-Diphenyl-9,9’-spirobifluoreno[2,3-c]thiophene (11d)
This is prepared essentially the same as 11a by employing 10d (0.6 g, 1.14 mmol); wet Pd/C (10%) 0.4 g
and xylenes (20 mL). It was purified (CH2Cl2 : PE = 1 : 6) as a white solid (0.22 g, 37%); Rf = 0.66 (PE :
CH2Cl2 = 1 : 4); mp 279-280 C. 1H NMR (CDCl3, 500 MHz, ppm) δ: 7.70-7.64 (m, 4H), 7.60-7.58 (m,
1H), 7.34 (d, J = 7.4 Hz, 2H), 7.27-7.26 (m, 1H), 7.19 (t, J = 7.1 Hz, 2H), 7.07 (t, J = 7.2 Hz, 2H),
6.99-6.90 (m, 6H), 6.79-6.72 (m, 3H), 6.49 (d, J = 6.9 Hz, 1H), 6.23 (d, J = 6.9 Hz, 2H); 13C NMR (125
MHz, CDCl3, ppm) δ: 150.82, 150.12, 141.70, 141.58, 140.54, 140.36, 138.93, 136.07, 135.51, 131.22,
129.81, 129.25, 128.97, 128.08, 128.04, 127.72, 127.31, 127.22, 127.10, 126.89, 125.83, 124.24, 124.01,
123.64, 119.66, 117.13, 117.06, 64.18. MS (EI): m/z = 374 [M-C12H6]+.
ACKNOWLEDGEMENTS
The authors thank the Shanghai Natural Science Foundation (09ZR1409400) of China and Shanghai
Committee of Science and Technology of China (10520710100) for financial support. We also thank the
large instruments open foundation of East China Normal University (2011-69) for instrument fund.
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