Org. Synth. 1995, 72, 232
DOI: 10.15227/orgsyn.072.0232
1-TRIFLUOROMETHYL-1-CYCLOHEXANOL
[Cyclohexanol, 1-(trifluoromethyl)-]
Submitted by Pichika Ramaiah, Ramesh Krishnamurti, and G. K. Surya Prakash
1.
Checked by Zhen-Yu Yang and Bruce E. Smart.
1. Procedure
CAUTION! All operations should be performed in a well ventilated hood. Hexaethylphosphorous triamide is potentially toxic and should be handled with protective gear.
A.
(Trifluoromethyl)trimethylsilane. A
2-L, three-necked flask is fitted with an
efficient, overhead, sealed mechanical stirrer, a
cold-finger condenser (30-cm in length and 8-cm in diameter) and a
rubber septum (Note 1). The top outlet of the condenser is attached to an
oil bubbler. The flask is flushed with dry
nitrogen and charged with
118.8 g (1.09 mol) of chlorotrimethylsilane (Note 2) in
100 mL of anhydrous benzonitrile (Note 3). The septum is replaced quickly under dry
nitrogen with a
500-mL Ace dry ice gas condenser trap (15-cm in length and 8-cm in diameter) (Note 4). The outlet of the trap is protected from moisture by a tube packed with
potassium hydroxide and the inlet is connected by tygon tubing to a cylinder of
bromotrifluoromethane (Note 5). The
2-L flask is immersed in a
dry ice-acetone bath maintained at −30°C
(Note 6) and the condensers are filled with dry ice-acetone mixture (−78°C). The cylinder is opened and 250 mL (d = 1.94 g/mL,
2 485 g, 3.25 mol) of bromotrifluoromethane is condensed into the
500-mL Ace reservoir (Note 7). Stirring is started, and the condensed liquid
bromotrifluoromethane is gradually added to the vessel at −30°C by slowly warming the reservoir to −45°C to −50°C. The resulting white slurry is further cooled to −60°C
(Note 6) and
(Note 8). The Ace dry ice gas condenser trap is disconnected under dry
nitrogen and replaced with a
600-mL, pressure-equalizing dropping funnel containing a solution of
325.0 g (1.31 mol) of hexaethylphosphorous triamide (Note 9) in
250 mL of dry benzonitrile. This solution is added with stirring at −60°C to the white slurry mixture over a period of 2.5 hr. After the addition is complete, the reaction mixture is stirred for an additional hour at −60°C
(Note 10), and then allowed to warm gradually to room temperature (25°C) over a period of 14 hr, during which time it turns clear yellow
(Note 11). The condenser and dropping funnel are removed and replaced by a
glass stopper and
joint adapter with its glass tube connected to two,
250-mL, dry ice/acetone-cooled traps; then aspirator vacuum (ca. 20 mm) is applied. The reaction flask is gently warmed to 50°C during which time (3 hr) all the volatile material collects in the cooled traps
(Note 12). The cooling baths are removed and the material in the traps is brought to 0°C. The colorless liquid is transferred quickly to a
250-mL separatory funnel, washed rapidly with ice cold water (3 × 100 mL), and the top organic product layer is separated
(Note 13). The product is dried over
5 g of anhydrous magnesium sulfate, and the dry liquid is decanted into a
250-mL flask. The product is fractionally distilled through a
15-cm column packed with glass helices. Three fractions are collected. The first minor fraction (bp
45–54°C) and the second major fraction (bp
54–55°C) contain the main quantity of
(trifluoromethyl)trimethylsilane. The third minor fraction (bp 55–65°C) consists mainly of
hexamethyldisiloxane with a small quantity of product
(trifluoromethyl)trimethylsilane (Note 14). The first and second fractions are combined to yield
116.9 g (
75%) of clear liquid product
(Note 15) and
(Note 16), bp
54–55°C (Note 17).
B. 1-Trifluoromethyl-1-cyclohexanol. A 250-mL, three-necked, round-bottomed flask equipped with a magnetic stirring bar, rubber septum, and a reflux condenser is attached to a nitrogen source to maintain a positive pressure and the other neck is closed with a glass stopper. Tetrahydrofuran (70 mL) (Note 18) and 19.2 g (0.13 mol) of (trifluoromethyl)trimethylsilane are introduced into the flask through the septum using dry syringes (Note 19). The flask is immersed in an ice-water bath (0°C), and a solution of 10.2 g (0.104 mol) of cyclohexanone (Note 20) in 50 mL of tetrahydrofuran is added to the stirred solution of (trifluoromethyl)trimethylsilane using a syringe. Tetrabutylammonium fluoride trihydrate (33 mg) catalyst (Note 21),(Note 22) is transferred into the reaction vessel. As the exothermic reaction proceeds, a yellowish brown color develops with the initial evolution of fluorotrimethylsilane (Note 23). The reaction mixture is stirred at 0°C for 30 min and then the cooling bath is removed. The reaction mixture is brought to room temperature and stirred for an additional hour. The reaction mixture is periodically analyzed by GC-MS and the reaction is complete within 1 hr at 25°C (Note 24). To the reaction mixture that contains crude 1-trifluoromethyl-1-O-(trimethylsilyl)cyclohexane are added 25 mL of tetrahydrofuran and 40 mL of 3 N hydrochloric acid. The mixture is stirred at room temperature for 8 hr and then transferred to a 500-mL separatory funnel containing 50 mL of water. The product is extracted with 50 mL of ether. The organic layer is separated and the aqueous layer is reextracted with 30 mL of ether. The combined organic layers are washed with 50 mL of water, dried over 10 g of anhydrous magnesium sulfate, and filtered. The residue is repeatedly washed with dry ether (3 × 20 mL). The solvent is removed on a rotary evaporator and the residue is dried to give a semi-solid that is purified by sublimation under vacuum (Note 25) to furnish 13.9–14.3 g (79–82%) of 1-trifluoromethyl-1-cyclohexanol as a white waxy solid, mp 60.8°C (Note 26).
2. Notes
1.
All glass apparatus is dried in an oven at 100°C and assembled while still hot under dry
nitrogen flow. All ground glass joints are tightly sealed with a Teflon tape and then wrapped with parafilm.
2.
Chlorotrimethylsilane (98%) was obtained from the Aldrich Chemical Company, Inc. and was distilled over
calcium hydride under a static atmosphere of dry
nitrogen just prior to use.
3.
Anhydrous
benzonitrile (99+%) was purchased from the Aldrich Chemical Company, Inc. and used without further purification.
4.
The trap was built in house. A
1000-mL Ace trap is available from the Aldrich Chemical Company, Inc.
5.
Bromotrifluoromethane, bp −57°C, was supplied by E.I. du Pont de Nemours & Co., Inc.6.
A temperature of −30°C to −60°C was maintained by adding dry ice to excess
acetone.
7.
The rate of
bromotrifluoromethane transfer was monitored by a
Nujol bubbler. A mark is made on the Ace reservoir trap to indicate the 250-mL volume.
8.
If the temperature falls below −60°C, the reaction mixture solidifies but returns to a liquid upon warming. The inverse addition, i.e., addition of
chlorotrimethylsilane to
bromotrifluoromethane, causes formation of a solid block that impedes stirring.
9.
Hexaethylphosphorous triamide (97%) was obtained from the Aldrich Chemical Company, Inc., and used as received. It can be prepared from
diethylamine and
phosphorus trichloride following the literature procedure.
3 410.
An exothermic reaction usually begins after all the
hexaethylphosphorous triamide is introduced, and some of the
bromotrifluoromethane escapes through the bubbler.
11.
To recover excess unreacted
bromotrifluoromethane, a dry ice-acetone cooled trap is connected to the condenser outlet before the reaction mixture is warmed to room temperature.
12.
The proton NMR of the distillate shows the two methyl group absorptions of
(trifluoromethyl)trimethylsilane and
chlorotrimethylsilane in a ratio of about 85:15. The material solidifies in a dry ice-acetone cooled trap.
13.
The distillate is shaken well with water to convert
chlorotrimethylsilane to
hexamethyldisiloxane.
14.
The product from the third fraction could not be isolated pure by redistillation.
15.
The yield is based on
chlorotrimethylsilane. A comparable yield of
77% was obtained when the reaction was repeated on one-third the scale. GC and NMR analyses show the product to be 98–99% pure.
16.
(Trifluoromethyl)trimethylsilane has the following spectroscopic properties:
1H NMR (200 MHz, CDCl
3) δ: 0.25 (s, 9 H, Si(CH
3)
3);
13C NMR (50.0 MHz, CDCl
3) δ: 131.7 (q,
1J
13C-
19F = 321.9), −5.2 (CH
3-Si);
19F NMR (188.0 MHz, CDCl
3, CFCl
3 external) d: −66.1;
29Si NMR (39.7 MHz, CDCl
3) δ: +4.7 (q,
2J(
29Si-
19F) = 37.9). MS (m/z) 123 (M
+-19).
17.
The boiling point for
(trifluoromethyl)trimethylsilane is reported as 45°C.
5 The submitters report a boiling point of 55.5°C.
18.
Reagent grade tetrahydrofuran was purchased from the Fisher Scientific Company and freshly distilled from
sodium benzophenone ketyl under dry
nitrogen atmosphere.
19.
Prior to use, the hypodermic syringes and needles were dried for several hours in an oven at 100°C and allowed to cool to ambient temperature in a desiccator.
20.
Cyclohexanone (99%) was purchased from the Aldrich Chemical Company, Inc., and used as such.
21.
Tetrabutylammonium fluoride (TBAF) trihydrate (99%) was purchased from the Aldrich Chemical Company, Inc.22.
TBAF trihydrate acts as an initiator and the water of hydration in TBAF does not pose any problem.
23.
Bubbles of
fluorotrimethylsilane are seen escaping during the initial stages of the reaction.
24.
Progress of the reaction can be monitored by GC-MS using a
Finnigan Model Incos-50 GC-MS spectrometer: Column: DB-5; temperature program: 50°C (4.5 min), 30°C/min, 250°C (30 min). Retention time:
Cyclohexanone, 7.44 min. and
1-trifluoromethyl-O-(trimethylsilyl)cyclohexane, 11.20 min.
25.
The product was sublimed at 2 mm at a bath temperature of 100°C. The receiver is cooled to 0°C, using an
ice-bath.
26.
The submitters report a melting point of
61.6°C. The product is pure (GC-MS) and has the following spectroscopic and analytical data : IR (KBr) cm
−1: 3364(s), 1255(s), 1146(s);
1H NMR (200 MHz, CDCl
3) δ: 1.00–1.90 (m,10 H), 1.93 (br, 1 H, OH);
13C NMR (50.0 MHz, CDCl
3) δ: 20.2, 25.0, 29.8, 72.6 (q,
2J
C-F = 28.2), 126.4 (q,
1J
C-F = 284.5 Hz, CF
3);
19F NMR (188 MHz, CDCl
3, CFCl
3, external) δ: −85.0; MS (m/z): 149 (M
+ -19, 0.57), 125 (1.25), 112 (1.23), 99 (100), 92 (1.50), 81 (66.79), 69 (10.49), 55 (26.01), 41 (37.26). Anal. Calcd for C
7H
11F
3O: C, 50.00; H, 6.59. Found: C, 49.69; H, 6.51.
Handling and Disposal of Hazardous Chemicals
The procedures in this article are intended for use only by persons with prior training in experimental organic chemistry. All hazardous materials should be handled using the standard procedures for work with chemicals described in references such as "Prudent Practices in the Laboratory" (The National Academies Press, Washington, D.C., 2011 www.nap.edu). All chemical waste should be disposed of in accordance with local regulations. For general guidelines for the management of chemical waste, see Chapter 8 of Prudent Practices.
These procedures must be conducted at one's own risk. Organic Syntheses, Inc., its Editors, and its Board of Directors do not warrant or guarantee the safety of individuals using these procedures and hereby disclaim any liability for any injuries or damages claimed to have resulted from or related in any way to the procedures herein.
3. Discussion
(Trifluoromethyl)trimethylsilane has been prepared by a modification
6 7 of the procedure originally published by Ruppert.
5 The optimized yield is 75%. Other less convenient methods are also available for its preparation.
8 9 (Trifluoromethyl)trimethylsilane acts as an in situ
trifluoromethide equivalent under nucleophilic initiation and reacts with a variety of electrophilic functional groups. Carbonyl compounds such as aldehydes, ketones and lactones react rather readily
6,7,10 with
(trifluoromethyl)trimethylsilane under fluoride initiation. The reagent also reacts with oxalic esters,
11 sulfonyl fluorides,
12 α-keto esters,
13 fluorinated ketones,
14 and sulfoxides.
15 Homologous trifluoromethyltrialkylsilanes have also been used as nucleophilic trifluoromethylating agents.
16 In the presence of
copper(I) iodide (CuI), homologous
(trifluoromethyl)triethylsilane reacts with aromatic, allylic and benzylic halides to provide the corresponding trifluoromethyl derivatives.
17 The synthetic applications of
trifluoromethyltrimethylsilane have been reviewed.
18 19
Appendix
Chemical Abstracts Nomenclature (Collective Index Number);
(Registry Number)
sodium benzophenone ketyl
1-Trifluoromethyl-1-O-(trimethylsilyl)cyclohexane
Tetrabutylammonium fluoride (TBAF) trihydrate
1-trifluoromethyl-O-(trimethylsilyl)cyclohexane
trifluoromethide
hydrochloric acid (7647-01-0)
ether (60-29-7)
benzonitrile (100-47-0)
Cyclohexanone (108-94-1)
nitrogen (7727-37-9)
acetone (67-64-1)
potassium hydroxide (1310-58-3)
phosphorus trichloride (7719-12-2)
diethylamine (109-89-7)
copper(I) iodide (7681-65-4)
magnesium sulfate (7487-88-9)
Tetrahydrofuran (109-99-9)
calcium hydride (7789-78-8)
Hexaethylphosphorous triamide (2283-11-6)
CHLOROTRIMETHYLSILANE (75-77-4)
hexamethyldisiloxane (107-46-0)
Tetrabutylammonium fluoride trihydrate (87749-50-6)
fluorotrimethylsilane (420-56-4)
1-Trifluoromethyl-1-cyclohexanol,
Cyclohexanol, 1-(trifluoromethyl)- (80768-55-4)
bromotrifluoromethane (75-63-8)
(Trifluoromethyl)trimethylsilane,
trifluoromethyltrimethylsilane (81290-20-2)
(trifluoromethyl)triethylsilane (120120-26-5)
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