1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL
1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL Basic information
- Product Name:
- 1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL
- Synonyms:
-
- 1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL
- 1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHANOL
- 3,5-BIS(TRIFLUOROMETHYL)-A-METHYLBENZYL ALCOHOL
- ALFA-METHYL-3,5-DITRIFLUOROMETHYLBENZYL ALCOHOL
- alpha-Methyl-3,5-bis(trifluoromethyl)benzyl alcohol
- 3,5-Bis(trifluoromethyl)phenylethanol
- alpha-Methyl-3,5-Bis(trifluoromethyl)Benzylalcohol99+%
- à-Methyl-3,5-bis-(trifluoromethyl)-benzyl alcohol
- CAS:
- 368-63-8
- MF:
- C10H8F6O
- MW:
- 258.16
- Product Categories:
-
- PHARMACEUTICAL INTERMEDIATES
- Aromatic alcohols and diols
- Mol File:
- 368-63-8.mol
1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL Chemical Properties
- Melting point:
- 70-74℃
- Boiling point:
- 175.8±35.0 °C(Predicted)
- Density
- 1.376±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 13.99±0.20(Predicted)
- Appearance
- White to off-white Solid
- CAS DataBase Reference
- 368-63-8(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Hazard Note
- Irritant
- HS Code
- 2906290090
1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL Usage And Synthesis
Synthesis
30071-93-3
7480-35-5
368-63-8
The general procedure for the synthesis of (R)-1-[3,5-bis(trifluoromethyl)phenyl]ethanol from 3,5-bis(trifluoromethyl)acetophenone and cis-1-amino-2,3-dihydro-1H-inden-2-ol is as follows: Example 5: To 2-propanol (21 L), [RuCl2 (p-cymene)]2 (18.4 g), (1S,2R)-cis-1-amino-2,3-dihydro-1H-inden-2-ol (9.0 g), and 1-(3,5-bis(trifluoromethyl)phenyl)ethan-1-one (3 kg) were added, stirred for 30 minutes and thoroughly degassed under vacuum. Subsequently, 5M sodium hydroxide solution (28mL) was added and the mixture was aged for 4-6 hours to ensure complete conversion of the feedstock. Upon completion of the reaction, the reaction mixture was poured into 1N HCl (21 L) and extracted with heptane (2 x 10.5 L). The organic layers were combined, washed with brine, and 1,4-diazabicyclo[2.2.2]octane (740 g) was added. The solution was concentrated to nearly 4 mL/g of alcohol (KF < 200 μg/mL; 2-propanol < 5 vol%). After inoculation at 40°C, the mixture was allowed to cool to room temperature to form crystalline species, which were further cooled to 0°C. The crystalline product was obtained by filtration, washed with cold heptane and dried to give the final DABCO complex in 75-80% yield and ee value >99%.
References
[1] Patent: US2002/22725, 2002, A1
[2] Patent: US2002/52493, 2002, A1
[3] Patent: US2002/52494, 2002, A1
[4] Patent: US6432952, 2002, B1
[5] Patent: US2003/215456, 2003, A1
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