A mild and efficient alternative to the classical swern oxidation

Full text of DOI:10.1021/jo015935s

J . Org. Chem. 2001, 66, 7907-7909
7907
A Mild a n d Efficien t Alter n a tive to th e
Sch em e 1
Cla ssica l Sw er n Oxid a tion
Lidia De Luca, Giampaolo Giacomelli,* and
Andrea Porcheddu
Dipartimento di Chimica, Universit a` degli Studi di Sassari,
Via Vienna 2, I-07100 Sassari, Italy
ggp@ssmain.uniss.it
Received J uly 17, 2001
Carbonyl compounds are of great importance as inter-
mediates to prepare other functional groups in organic
synthesis. In particular, aldehydes and N-protected
R-amino aldehydes1 are important and versatile com-
pounds.
sulfoxide (DMSO), activated by 2,4,6-trichloro[1,3,5]-
triazine (cyanuric chloride, TCT), under the so-called
Swern oxidation conditions.10
Oxidation of alcohols to the corresponding carbonyl
compounds is one of the most important synthetic
procedures, and the development of selective and efficient
reagents for that conversion, especially when other
oxidizable functional groups are also present, has inter-
ested organic chemists for a long time. In this context,
notwithstanding the availability of many preparative
methods, the restrictions that accompany some of them
make new, mild, and selective procedures highly desir-
able. Most of the methods for the oxidation of alcohols
utilize dimethyl sulfoxide as a reagent via dimethyl
alkoxysulfonium salts that react with a base to give the
carbonyl compound and dimethyl sulfide. The electro-
philic reagents that have been used to activate dimethyl
We have observed that the activation of DMSO can be
conveniently conducted with the very cheap cyanuric
chloride, which can be used even for large-scale work,
simply using THF as solvent. The procedure is based on
treatment of TCT with 5 equiv of DMSO in THF at -30
°
C for 30 min, followed by addition of the alcohol. After
an additional 30 min, triethylamine (TEA, 4 equiv) was
added (Scheme 1). The reaction mixture was then
quenched with water and worked up to yield the carbonyl
compound. Although formation of the dimethyl alkoxy-
sulfonium salt occurred even at 0 °C without any appar-
ent decomposition, the reactions were carried out at -30
2
sulfoxide include acetic anhydride, methanesulfonic
°
C to prevent eventual formation of undesirable byprod-
anhydride,3 tosyl chloride, sulfur trioxide/pyridine,5
phosphorus pentoxide, thionyl chloride,7 and oxalyl
chloride7 among others. Generally, the activation of
DMSO can be violent and exothermic, and successful
activation requires low temperatures, usually -60 °C. Of
all the activators, the highest yields of carbonyl com-
pounds, with minimal byproduct formation, were ob-
tained with thionyl chloride and oxalyl chloride, espe-
cially the latter. Unfortunately, oxalyl chloride is moisture
sensitive and dangerously toxic, and its vapor is a
powerful irritant, particularly to the respiratory system
and to the eyes.
4
11
ucts, such as chloro derivatives or thiomethyl ethers.
As shown in Tables 1 and 2, a variety of carbonyl
compounds and N-protected amino aldehydes were pre-
pared from commercially available alcohols. The yields
6
,8
12
were quantitative (>99%), and the conversion was very
high in most of the cases. The oxidation proceeds with
satisfactory rates even when the alcohol has steric
constrains. Only in the case of 9-fluorenemethanol was
the reaction found to be very slow (20% conversion after
8
h). The oxidation of 2-phenylthioethanol is very slow
too, possibly due to the competition of sulfur atom of the
alcohol in the coordination with the TCT.
On this basis and following our interest in the use of
The methodology is cleanly applicable to N-protected
9
[
1,3,5]triazine derivatives in organic synthesis, herein
13
â-amino alcohols: the corresponding aldehydes are
we report a mild and efficient alternative procedure for
the quantitative conversion of alcohols into the corre-
sponding carbonyl compounds. The method uses dimethyl
recovered as pure products and in good conversions even
if the reaction requires a longer time (90 min after the
addition of TEA). Only N-Boc â-amino alcohols seem to
react more slowly and in some cases may deprotect
partially under the reaction conditions (e.g., Table 2, run
3).
(
(
(
(
(
1) J urczak, J .; Golebiowski, A. Chem. Rev. 1989, 89, 149.
2) Albright, J . D.; Goldman, L. J . Org. Chem. 1967, 32, 2416.
3) Murray, R. W.; Gu, D. J . Chem. Soc., Perkin Trans. 2 1994, 451.
4) Albright, J . D. J . Org. Chem. 1974, 39, 1977.
On these results, R-amino aldehydes could be ef-
5) Parikh, J . R.; Doering, W. Von E. J . Am. Chem. Soc. 1967, 89,
ficiently prepared in total good yield by using TCT/NaBH
4
5
507.
reduction9 of N-protected R-amino acid followed by
a
(
6) Taber, D. F.; Amedio, J . C., J r.; J ung, K. J . Org. Chem. 1987,
5
2, 5621.
(
(
7) Omura, K.; Swern, D. Tetrahedron 1978, 34, 1651.
8) Marx, M.; Tidwell, T. T. J . Org. Chem. 1984, 49, 788. Liu, Y.;
(10) The use of TCT was already cited but the author reported only
two examples, where TCT was used dissolved in a very toxic, possibly
carcinogenic solvent such as HMPA.
(11) Mancuso, A. J .; Swern, D. Synthesis 1981, 165.
(12) Determined by NMR analysis of the crude product after 30 min
of the addition of TEA.
Vederas, J . C. J . Org. Chem. 1996, 61, 7856.
9) (a) Falorni, M.; Porcheddu, A.; Taddei, M. Tetrahedron Lett. 1999,
0, 4395. (b) Falorni, M.; Giacomelli, G.; Porcheddu, A.; Taddei, M. J .
4
(
4
Org. Chem. 1999, 64, 8962. (c) Falchi, A.; Giacomelli, G.; Porcheddu,
A.; Taddei, M. Synlett 2000, 275. (d) De Luca, L.; Giacomelli, G.;
Taddei, M. J . Org. Chem. 2001, 66, 2534. (e) De Luca, L.; Giacomelli,
G.; Porcheddu, A. Org. Lett. 2001, 3, 1519.
(13) In the case of N-Fmoc R-amino alcohol, diisopropylethylamine
(DIPEA) was used instead of TEA.
1
0.1021/jo015935s CCC: $20.00 © 2001 American Chemical Society
Published on Web 10/12/2001

7
908 J . Org. Chem., Vol. 66, No. 23, 2001
Notes
Ta ble 1. Con ver sion of Alcoh ols in to th e Cor r esp on d in g
Ca r bon yl Com p ou n d s
Ta ble 2. Con ver sion of N-P r otected r-Am in o Alcoh ols
in to N-P r otected r-Am in o Ald eh yd es
a
After 90 min from addition of the tertiary amine. b The
compound was recovered partially deprotected (25%).
Exp er im en ta l Section
All the solvents and the reagents were used in the com-
mercially available grade of purity. The N-protected â-amino
alcohols were prepared from the corresponding R-amino acids
according to the literature,9b and their purity was established
before utilization by melting point and optical rotation. Cyanuric
chloride was purchased from Avocado.
Elemental analyses were performed on a Perkin-Elmer 420
B analyzer, optical rotations were measured with a Perkin-Elmer
1
2
41 automatic polarimeter in a 1 dm tube. The H NMR (300
1
3
MHz) and C NMR (75.4 MHz) were obtained with a Varian
VXR-300 spectrometer from CDCl solutions.
3
Gen er a l P r oced u r e for th e Syn th esis of Ald eh yd es a n d
Ket on es. The procedure for the preparation of N-benzyloxy-
carbonyl-2-amino-3-phenylpropionaldehyde is representative.
DMSO (1.25 mL, 17.6 mmol) was added to a solution of TCT
(0.66 g, 3.6 mmol) in THF (20 mL) stirred and maintained at
a
b
After 30 min from addition of TEA. The compound polymer-
c
izes when pure. Conversion after 8 h.
-
30 °C. After 30 min, N-benzyloxycarbonyl-2-amino-3-phenyl-
2
0
propan-1-ol, [R]
D
- 41.0 (c 1, MeOH) (0.86 g, 3 mmol), in THF
oxidation according to the present procedure. Thus, (S)-
N-benzyloxyca rbon yl-2-a m in o-3-ph enylpropiona lde-
(10 mL) was added slowly at -30 °C with stirring, followed by
TEA (2 mL, 14.3 mmol) after an additional 30 min. After 15 min,
the mixture was warmed to room temperature, the solvent
hyde, [R]20
-52.3 (c 0.7, MeOH) was recovered, without
14
D
evaporated under vacuum, and Et O (50 mL) added to the solid
formed. The mixture was quenched with 1 N HCl, and the
organic phase washed with 15 mL of a saturated solution of
2
significant racemization of the chiral center, from (S)-
N-benzyloxycarbonylphenylalanine. This method could
avoid some problems encountered in the synthesis of the
aldehydes by controlled DIBAL reduction of R-amino
NaHCO
Na SO
carbonyl-2-amino-3-phenylpropionaldehyde (0.77 g, 90%): mp
3
, followed by brine. The organic layer was dried
(
2
4
) and the solvent evaporated to yield pure N-benzyloxy-
esters15 or in the reduction of N-protected R-amino acids
and Pd/C.9
b
20
D
14 1
by H
2
79 °C; [R]
- 52.3 (c 0.7, MeOH);
H NMR δ 9.63 (s, 1H),
7
2
.37 (m, 10H), 5.31 (s, 1H), 5.11 (s, 2H), 4.50 (m, 1H), 3.15 (d,
In conclusion, the method presented in this report is
operationally simple and can be used as a valid alterna-
tive to the classical Swern oxidation, requiring milder
conditions and cheaper reagents.
H).
Simple aldehydes and ketones obtained were characterized
by usual spectral data and compared with authentical samples,
when commercial, or with the literature values. The following
R-amino aldehydes were already described: N-benzyloxycar-
bonylglycinal,16 N-tert-butoxycarbonyl-L-phenylalaninal,
14b,17
N-
(14) (a) Sharma, R. P.; Gore, M. G.; Akhtar, M J . Chem. Soc., Chem.
Commun. 1979, 875. (b) Soucek, M.; Urban, J Collect. Czech. Chem.
Commun. 1995, 60, 693.
(16) Hamada, Y.; Shibata, M.; Sugiura, T.; Kato, S.; Shioiri, T. J .
Org. Chem. 1987, 52, 1252.
(15) Garner, P.; Park, J . M. Org. Synth. 1991, 70, 18. Roush, W. R.;
Hunt, J . A. J . Org. Chem. 1995, 60, 798.
(17) Castro, B.; Fehrentz, J . A. Synthesis 1983, 676.

Notes
tert-butoxycarbonyl-L-isoleucinal, N-benzyloxycarbonyl-L-vali-
J . Org. Chem., Vol. 66, No. 23, 2001 7909
1
7
(m, 4H); 13C NMR δ 199.4, 157.4,140.1, 132.6, 128.2, 124.9, 120.8,
67.0, 64.8, 47.2 46.3, 27.6, 23.5. Anal. Calcd for C20H19NO
3
(321.14): C, 74.75; H, 5.96; N, 4.36. Found: C, 74.75; H, 5.99;
N, 4.34.
1
6
18
nal, N-(9-fluorenylmethoxycarbonyl)-L-phenylalaninal, N-
1
4
benzyloxycarbonyl-L-prolinal.
N-(9-F lu or en ylm eth oxyca r bon yl)-L-p r olin a l (0.83 g,
1
8
8
6%): H NMR δ 9.44 (s, 0.6H), 9.13 (s, 0.4H), 7.82-7.23 (m,
Ack n ow led gm en t. The work was financially sup-
ported by the University of Sassari (Fondi 60%).
H) 4.47-3.98 (m, 3H), 3.89 (m, 1H), 3.40 (m, 2H), 2.03-1.60
(18) Wen, J . J .; Crews, C. M. Tetrahedron: Asymmetry 1998, 9, 1855.
J O015935S