| Identification | Back Directory | [Name]
(S)-1,1,1-TRIFLUORO-2-PROPANOL | [CAS]
3539-97-7 | [Synonyms]
(S)-Trifluoroisopropanol
(S)-1,1,1-Trifluoropropan-2-ol
(2S)-1,1,1-Trifluoropropan-2-ol
(2S)-1,1,1-trifluoro-2-propanol
2-Propanol, 1,1,1-trifluoro-, (2S)-
(2S)-2-Hydroxy-1,1,1-trifluoropropane
(S)-1,1,1-TRIFLUORO-2-PROPANOL (2S)-1,1,1- | [Molecular Formula]
C3H5F3O | [MDL Number]
MFCD06797331 | [MOL File]
3539-97-7.mol | [Molecular Weight]
114.07 |
| Chemical Properties | Back Directory | [Boiling point ]
67.0±35.0℃ (760 Torr) | [density ]
1.235±0.06 g/cm3 (20 ºC 760 Torr) | [Fp ]
38.8±17.0℃ | [form ]
liquid | [pka]
12.53±0.20(Predicted) | [color ]
Clear | [InChI]
InChI=1S/C3H5F3O/c1-2(7)3(4,5)6/h2,7H,1H3/t2-/m0/s1 | [InChIKey]
GILIYJDBJZWGBG-REOHCLBHSA-N | [SMILES]
C(F)(F)(F)[C@@H](O)C |
| Hazard Information | Back Directory | [Description]
(S)-1,1,1-Trifluoro-2-propanol is a compound important as an intermediate for various medicines and agrichemicals. Aside from methods using chemical catalysts, biological methods of reducing 1,1,1-trifluoroacetone to (S)-1,1,1-trifluoro-2-propanol by having microbial enzymes act on 1,1,1-trifluoroacetone has hitherto been studied. | [Uses]
(S)-1,1,1-TRIFLUORO-2-PROPANOL can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development and chemical production processes. | [Synthesis]
A liquid medium was prepared to be composed of 2000 ml of an ion-exchanged water, 60 g of glucose, 30 g of peptone, 50 g of yeast extract, 4.8 g of potassium dihydrogenphosphate and 2.5 g of dipotassium hydrogen phosphate. The liquid medium was charged into a fermenter of 5 L capacity (available from B.E. MARUBISHI Co., Ltd. under the trade name of a MDN-type 5L(S)) and then subjected to steam sterilization at 121°C for 60 minutes. This liquid medium was inoculated with 80 ml of a suspension of Hansenula polymorpha NBRC0799, the suspension being obtained by conducting a preliminary culture on 100 ml of the same composition to be 2.0 × 109 cfu/ml. Then, it was cultured at 28°C, an air ventilation of 1 vvm and a stirring speed of 500 rpm for 24 hours, thereby preparing a suspension of 4.3 × 109 cfu/ml (or 86 g/L in terms of the weight of wet cell bodies). At this time, adjustment of pH was attained by using aqueous ammonia, so that a pH was adjusted at 6.5. After culture had terminated, the ventilation amount and the stirring speed were changed to 0.1 vvm and 50 rpm. A solution obtained by dissolving 125.2 g of 1,1,1-trifluoroacetone and 200 g of glucose in 300 ml of an ion-exchanged water prepared in another vessel was added to the suspension automatically by a computer program in the use of an online sugar concentration sensor (an online biosensor available from ABLE & Biott Co.,Ltd. under the trade name of BF-410), so as to maintain a glucose concentration of 2 %. It was confirmed that the yield obtained after a lapse of 168 hours was 94.9 % by monitoring the reduction of the substrate due to the microorganism every 24 hours, upon which the reaction was terminated.
In order to recall 1,1,1-trifluoro-2-propanol produced from the reaction solution after termination of the reaction, distillation was performed. A distillate was recalled in an amount of 188 ml, from which it was found, by internal standard method of 19F-NMR, that 109.2 g of 1,1,1-trifluoro-2-propanol was contained. As a result of measuring the optical purity under the above-discussed analyzing conditions, the optical purity was confirmed to be 98.7% ee (S-configuration). |
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