Aminodifluorosulfinium Tetrafluoroborate salts as stable and crystalline deoxofluorinating reagents

Article abstract of DOI:10.1021/ol902039q

Aminodifluorosulfinium tetrafluoroborate salts were found to act as efficient deoxofluorinating reagents when promoted by an exogenous fluoride source and, In most cases, exhibited greater selectivity by providing less elimination byproduct as compared to DAST and DeoxoFluor. Aminodifluorosulfinium tetrafluoroborates are easy handled crystalline salts that show enhanced thermal stability over dialkylaminosulfur trifluorides, are storage-stable, and unlike DAST and Deoxo-Fluor do not react violently with water.

Full text of DOI:10.1021/ol902039q

ORGANIC
LETTERS
2
009
Vol. 11, No. 21
050-5053
Aminodifluorosulfinium
Tetrafluoroborate Salts as Stable and
Crystalline Deoxofluorinating Reagents
5
Francis Beaulieu, Louis-Philippe Beauregard, Gabriel Courchesne,
Michel Couturier,* Fran c¸ ois LaFlamme, and Alexandre L’Heureux
OmegaChem Inc., 8800 Boul. De la RiVe-Sud, L e´ Vis, QC G6V 9H1, Canada
michelcouturier@omegachem.com
Received September 3, 2009
ABSTRACT
Aminodifluorosulfinium tetrafluoroborate salts were found to act as efficient deoxofluorinating reagents when promoted by an exogenous
fluoride source and, in most cases, exhibited greater selectivity by providing less elimination byproduct as compared to DAST and Deoxo-
Fluor. Aminodifluorosulfinium tetrafluoroborates are easy handled crystalline salts that show enhanced thermal stability over dialkylaminosulfur
trifluorides, are storage-stable, and unlike DAST and Deoxo-Fluor do not react violently with water.
3
Fluorines are of high importance in pharmaceuticals and
agrochemicals because their presence in organic molecules
can advantageously alter their chemical and biological
profiles, including stability, lipophilicity, and bioavailability.
In fact, 30-40% of agrochemicals and 20% of pharmaceu-
gaseous SF
4
. Unfortunately, it was soon recognized that this
4
liquid was thermally unstable and highly explosive in nature.
In an effort to develop a safer reagent, Lal et al. have reported
that bis(2-methoxyethyl)aminosulfur trifluoride (Deoxo-
5
Fluor, 2) was more thermally stable. In this context, it has
1
ticals on the market are estimated to contain fluorine atoms.
been shown by differential scanning calorimetry (DSC) that
DAST and Deoxo-Fluor have the same decomposition
temperature, but DAST degrades more rapidly with some-
what larger heat evolution.
As such, there is an increasing need for safe, selective, and
efficient methods to introduce fluorine atoms in molecules,
and a common practice is to produce fluorides from alcohols
and gem-difluorides from carbonyl functional groups. These
transformations are commonly referred to as deoxofluori-
nations.
DAST (1) and Deoxo-Fluor (2) are the most widely used
deoxofluorinating reagents. These reagents are fuming
liquids that are difficult to handle in humid environments,
react violently with water, and do not offer the convenience
of handling solids from a manufacturing standpoint. The
liquids also discolor with aging and sometimes require
6
It was recognized early that SF
4
can perform deoxoflu-
orinations, but in practice, handling of this highly toxic gas
2
necessitates extensive safety measures. Reactions using SF
4
7
are often undertaken under pressure, require high tempera-
tures (typically 100 °C), and lead to undesired products.
Later, liquid-state diethylaminosulfur trifluoride (DAST, 1)
was developed by Middleton as a superior alternative to
redistillation to be satisfactory. As a consequence of their
(
3) Middleton, W. J. J. Org. Chem. 1975, 40, 574.
(4) (a) Cochran, J. Chem. Eng. News 1979, 57 (12), 74. (b) Middleton,
W. J. Chem. Eng. News 1979, 57 (21), 43. (c) Messina, P. A.; Mange,
K. C.; Middleton, W. J. J. Fluor. Chem. 1989, 42, 137.
(5) Lal, G. S.; Pez, G. P.; Pesaresi, R. J.; Prozonic, F. M.; Cheng, H. J.
Org. Chem. 1999, 71, 7048.
(
(
1) Thayer, A. M. Chem. Eng. News 2006, 84 (23), 15.
2) Hasek, W. R.; Smith, W. C.; Engelhardt, V. A. J. Am. Chem. Soc.
1
960, 82, 543.
(6) Singh, R. P.; Shreeve, J. M. Synthesis 2002, 17, 2561.
10.1021/ol902039q CCC: $40.75
Published on Web 10/02/2009
 2009 American Chemical Society

Figure 1. Structures of popular dialkylaminosulfur trifluorides.
explosiveness, DAST-type reagents are subject to strict legal
provisions and shipping restrictions. There is therefore a need
for deoxofluorinating reagents that do not suffer from the
aforementioned deficiencies of dialkylaminosulfur trifluo-
rides. Ideally, the deoxofluorinating reagents would be stable
from handling, storage, and process safety standpoints, would
be cost-efficient, and could be prepared in high yield and
isolated efficiently in a solid-state form by simple filtration.
Herein, we report that dialkylaminodifluorosulfinium salts
can be employed as surrogates of aminosulfur trifluorides
and provide a safer alternative reagent thereof.
Figure 2. Dialkylaminodifluorosulfinium salts.
74-76 °C using the same solvent. The recrystallized material
exhibits better handling properties, can be manipulated in
1
2
ambient conditions, and is storage-stable.
We next assessed the thermal stability by performing a
preliminary hazard study of diethylaminodifluorosulfinium
tetrafluoroborate (4). DSC analysis showed a decomposition
temperature at 215 °C with an exothermic heat (-∆H) of
Distinctly isolated and characterized dialkylaminodifluo-
rosulfinium salts have been known for over three decades.
Markovskii et al. first reported that DAST (1) and the
dimethylamino, piperidino, and morpholino analogues all
6
61 J/g. In comparison, DAST decomposes at 140 °C,
releasing 1700 J/g, and Deoxo-Fluor decomposes at 140 °C
with 1100 J/g of energy. In general, a higher decomposition
5
temperature and a lower exothermic heat generated during
decomposition is indicative of a more stable compound and
provides greater safety.
react with BF
nodifluorosulfinium tetrafluoroborates 3-6.
initial discovery, other dialkylaminodifluorosulfinium salts
7-9) have been reported, all of which were prepared by
the reaction of a DAST-type reagent with fluoride ion
3
2
·Et O to form the corresponding dialkylami-
8
,9
Since this
(
The physical attributes and the thermal stability of morpholino
and bis(2-methoxyethyl)aminodifluorosulfinium tetrafluorobo-
rate salts were also investigated. DSC analysis of the latter (11)
showed decomposition at 193 °C with a release of 367 J/g.
Although less energetic than the diethylamino analogue 4, the
decomposition occurs at a lower temperature. Moreover, the
salt 11 has a low melting point of 35-38 °C, is highly
hygroscopic, deliquescent, and as such, not easily handled. On
the other hand, the morpholino analogue 6 has a high melting
point of 122-125 °C and is more stable on the basis of both
decomposition temperature and amount of energy released. In
fact, morpholinodifluorosulfinium tetrafluoroborate (6) decom-
posed at 242 °C while releasing only 388 J/g, which favorably
compares to Deoxo-Fluor (140 °C with 1100 J/g).
10
acceptors such as BF
fluorination of silylamines,
3
, PF
5
, SeF
4
, SbF
5
, and AsF
5
. Besides
8
,10d
the reactivity of dialkylami-
nodifluorosulfinium salts as reagents has been scarcely
studied. To the best of our knowledge, not a single deox-
ofluorination reaction of an alcohol, aldehyde, ketone, or
carboxylic acid has ever been reported. Moreover, their
thermal stability has not been evaluated.
To further investigate the properties of dialkylaminodif-
luorosulfinium salts, several derivatives were prepared using
a modified version of the original Markovskii procedure,
including the novel salt 11 derived from Deoxo-Fluor. We
were pleased to observe the ease at which dialkylaminodi-
fluorosulfinium tetrafluoroborate salts precipitated directly
out of solution upon the reaction of the corresponding
dialkylaminosulfur trifluorides and BF
facturing standpoint, this constitutes a direct-drop process,
3
2
·Et O. From a manu-
Table 1. Preparation of Dialkylaminodifluorosulfinium
Tetrafuoroborate Salts and DSC Analyses
1
1
which greatly simplifies the isolation procedure. In fact,
the solid-state salts are easily filterable and dried under inert
atmosphere. The DAST-derived salt 4 had an amorphous
appearance, was pale yellow and somewhat hygroscopic. The
crude salt was therefore recrystallized in 1,2-dichloroethane
to obtain white microcrystalline flakes melting at 83-84 °C,
whereas Markovskii reported obtaining needles melting at
DSC
compound
yield (%)
mp (°C)
Tdec (°C) -∆Hdec (J/g)
4
82
75
78
83-84
122-125
35-38
215
242
193
140
140
661
388
367
1700
1100
6
1
(
7) Fauq, A. H.; Singh, R. P.; Meshri, D. T. In Handbook of Reagents
1
for Organic Synthesis-Fluorine Containing Reagents; Paquette, L. A., Ed.;
DAST
Deoxo-Fluor
John Wiley & Sons Ltd.: England, 2007; pp 180-194.
(
8) Markovskii, L. N.; Pashinnik, V. E.; Saenko, E. P. Zh. Org. Khim.
1
977, 13, 1116
.
Org. Lett., Vol. 11, No. 21, 2009
5051

Since the reactivity of aminodifluorosulfinium salts toward
hydroxyls and carbonyls was unknown as of yet, the potential
use of such salts as deoxofluorinating reagents was next
assessed. In preliminary trials, we found that diethylamin-
odifluorosulfinium tetrafluoroborate (4) alone was incapable
of performing deoxofluorination of carbonyls, whereas
alcohols did convert into the desired fluorides, albeit slug-
gishly. For example, when 4-tert-butylcyclohexanone was
treated with the foregoing salt, no detectable conversion to
Table 2. Deoxofluorinations Using
Diethylaminodifluorosulfinium Tetrafuoroborate 4
,
a b
1-tert-butyl-4,4-difluorocyclohexane was observed even after
4
days at room temperature. This result was unexpected since
Lal et al. had claimed that BF
3 2
·Et O catalyzes the dialky-
laminosulfur trifluoride mediated deoxofluorination of ke-
1
3
tones. However, Merck has reported that 10 mol % of
BF ·Et O substantially retards the rate of reaction in the
deoxofluorination of a ketone by Deoxo-Fluor. All indica-
tions suggest that BF ·Et O does not act as a Lewis acid but
3
2
14
3
2
rather as an irreversible fluoride ion acceptor to form
dialkylaminodifluorosulfinium tetrafluoroborate salts with
attenuated reactivity.
From a mechanistic perspective, it is recognized that
the reaction of DAST and alcohols produces a dialky-
laminodifluorosulfane intermediate along with HF, the
latter of which serves as a fluoride source for the final
displacement in the synthetic pathway leading to the alkyl
3
,15
fluoride.
By analogy, we surmised that the electrophilic
dialkylaminodifluorosulfinium species is capable of reacting
with an alcohol to provide an alkoxy-N,N-dialkylaminodif-
luorosulfane, but since tetrafluoroboric acid is released
instead of the requisite HF, the overall process cannot be
completed. In this context, an exogenous source of fluoride
would be required.
After much investigation, we were pleased to observe that
complete conversion of 3-phenylpropanol to 1-fluoro-3-
phenylpropane could be achieved when the reaction was
a
b
Isolated yield. Combined yield of product and elimination side product
(
the percentage yield of side product in the isolated mixture calculated from
H and F NMR).
1
19
performed in the presence of 3HF·Et
, entry 1). It is noteworthy that, unlike Olah’s reagent (i.e.,
pyridinium polyhydrogen fluoride) and anhydrous hydrogen
fluoride, 3HF·Et N is much less corrosiVe, is almost pH
neutral, and can be handled in borosilicate glassware up to
3
N as a promoter (Table
2
17
(
Table 2). An additional advantage of diethylaminodifluo-
rosulfinium tetrafluoroborate over DAST and Deoxo-Fluor
became apparent in the deoxofluorination of 4-tert-butylcy-
clohexanone (entry 4). Typically, a major side reaction
observed in the deoxofluorination of ketones is the production
of the corresponding olefinic fluoride side product. In fact,
the reactions of DAST/HF and Deoxo-Fluor/HF with 4-tert-
butylcyclohexanone were reported to produce 33% and 16%
3
1
6
1
50 °C without corrosion.
Gratifyingly, the 3HF·Et
3
N-promoted deoxofluorination
using diethylaminodifluorosulfinium tetrafluoroborate was
found generally applicable to a wide variety of substrates
including alcohols, aldehydes, ketones, and carboxylic acids
5
of olefinic fluoride side product, respectively, whereas
diethylaminodifluorosulfinium tetrafluoroborate exhibited
higher selectivity by leading to only 4% of olefinic fluoride
using the same substrate.
(
9) Compounds 4 and 6 can be obtained from the Aldrich Chemical
Co. (catalogue nos. 719439 and 719447, respectively)
10) (a) Cowley, A. H.; Pagel, D. J.; Walker, M. L. J. Am. Chem. Soc.
978, 100, 7065. (b) Mews, R.; Henle, H. J. Fluor. Chem. 1979, 14, 495.
c) Pauer, F.; Erhart, M.; Mews, R.; Stalke, D. Z. Naturforsch., B: Chem.
(
1
(
Sci. 1990, 45, 271. (d) Pashinnik, V. E.; Martynyuk, E. G.; Shermolovich,
Y. G. Ukr. Khim. Zh. 2002, 68, 83.
(16) (a) Haufe, G. J. Prakt. Chem. 1996, 338, 99. (b) McClinton, M. A.
Aldrichimica Acta 1995, 28, 31. (c) Gatner, K. Pol. J. Chem. 1993, 67,
1155. (d) Franz, R. J. Fluorine Chem. 1980, 15, 423.
(
(
11) Anderson, N. G. Org. Process Res. DeV. 2004, 8, 260.
12) A sample of salt 4 stored at room temperature under inert nitrogen
(17) General procedure for deoxofluorination. To a stirred suspension
of diethylaminodifluorosulfinium tetrafluoroborate (4.0 mmol) in dichlo-
romethane (25 mL) at room temperature was added the substrate (2.67
mmol) and triethylamine trihydrofluoride (4.0 mmol). The resulting mixture
was stirred under nitrogen over the prescribed amount of time. The reaction
was then quenched at room temperature with a 5% sodium bicarbonate
aqueous solution and stirred for 15 minutes, and the resulting mixture was
extracted twice using dichloromethane. The organic phases were combined,
dried over magnesium sulfate, filtered, and concentrated. The residual oil
was analyzed after 90 days with no detectable degradation.
(
(
13) Lal, G. S.; Pez, G. P. U.S. patent 6,222,064 B1, 2001.
14) Mase, T.; Houpis, I. N.; Akao, A.; Dorzoitis, I.; Emerson, K.;
Hoang, T.; Iida, T.; Itoh, T.; Kamei, K.; Kato, S.; Kato, Y.; Kawasaki, M.;
Lang, F.; Lee, J.; Lunch, J.; Maligres, P.; Molina, A.; Nemoto, T.; Okada,
S.; Reamer, R.; Song, J. Z.; Tschaen, D.; Wada, T.; Zewge, D.; Volante,
R. P.; Reider, P. J.; Tomimoto, K. J. Org. Chem. 2001, 66, 6775.
(
15) (a) Tewson, T. J.; Welch, M. J. J. Org. Chem. 1978, 43, 1090. (b)
Sutherland, A.; Vederas, J. C. Chem. Commun. 1999, 1739
.
2
was purified by SiO chromatography.
5052
Org. Lett., Vol. 11, No. 21, 2009

As mentioned above, deoxofluorinations on six-membered
ring systems are notoriously prone to elimination, and the
monoprotected 1,4-cyclohexanedione 12 is no exception
We were pleased to observe, however, an 8-fold increase in
selectivity when promoted with 3HF·Et N with an isolated
yield of 63%.
3
1
8
(
Table 3). In fact, Deoxo-Fluor predominantly leads to
In summary, results of this preliminary investigation have
shown that dialkylaminodifluorosulfinium tetrafluoroborate
salts are considerably more stable than dialkylaminosulfur
trifluorides, both in terms of higher decomposition temper-
ature and lower amount of energy released. These salts are
capable of performing deoxofluorinations of hydroxyls and
carbonyls when promoted by an exogenous fluoride source,
Table 3. Case Study: Deoxofluorination Reaction Outcome of
Cyclohexanone 12
3
i.e., 3HF·Et N and, in most cases, led to fewer elimination
byproducts as compared to DAST and Deoxo-Fluor. These
desirable attributes, combined with the ease of handling and
storage stability of dialkyaminodifluorosulfinium tetrafluo-
roborate salts, make these reagents a useful and safer option
to perform deoxofluorination reactions, especially on a large
scale. Further investigations into mechanistic aspects and
substrate scope are currently underway and will be reported
in due course.
entry
reagent (equiv)
additive (equiv)
none
BF ·OEt (0.1)
3 2
3HF·TEA(0.3)
none
13:14 ratio
1
2
3
4
5
Deoxo-Fluor (1.2)
Deoxo-Fluor (1.2)
Deoxo-Fluor (1.2)
11 (2.0)
0.8:1
1.4:1
1.0:1
no conv
6.9:1
Acknowledgment. We thank Mahmoud Mirmehrabi (Wy-
eth Research, Canada) for conducting the DSC analyses.
11 (2.0)
3HF·TEA(1.0)
Supporting Information Available: Experimental pro-
cedures, characterization data, and copies of H, C, and
F NMR and DSC spectras. This material is available free
of charge via the Internet at http://pubs.acs.org.
olefinic fluoride 14, whereas the addition of promoters
modestly increases the selectivity. More specifically, 0.1
1
13
1
9
equiv of BF
3 2
·Et O almost doubles the selectivity, but
increasing further the amount of the additive slowed down
the reaction rate and led to intractable mixtures. Ultimately,
no conversion to 13 was observed when equimolar amounts
OL902039Q
3 2
of Deoxo-Fluor and BF ·Et O, i.e., the salt 11, was employed.
(18) Unoptimized yield of a mixture of 13 and 14.
Org. Lett., Vol. 11, No. 21, 2009
5053