Basic information Safety Supplier Related

1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL

Basic information Safety Supplier Related

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
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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)
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2906290090
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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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