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

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Products Intro: Product Name:3,5-Bis(trifluoromethyl)phenyl ethanol
CAS:368-63-8
Purity:0.98 Package:1G;1KG;100KG
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Products Intro: Product Name:1-(3,5-Bis(trifluoromethyl)phenyl)ethanol
CAS:368-63-8
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CAS: 368-63-8
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CAS:368-63-8
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Products Intro: Product Name:1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL
CAS:368-63-8
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1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL manufacturers

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
EINECS:
Product Categories:PHARMACEUTICAL INTERMEDIATES;Aromatic alcohols and diols
Mol File:368-63-8.mol
1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL Structure
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
pka13.99±0.20(Predicted)
AppearanceWhite to off-white Solid
CAS DataBase Reference368-63-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Hazard Note Irritant
HS Code 2906290090
MSDS Information
1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL Usage And Synthesis
Synthesis
3',5'-Bis(trifluoromethyl)acetophenone

30071-93-3

1-AMINO-2-HYDROXYINDANE

7480-35-5

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

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
Tag:1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL(368-63-8) Related Product Information
3,5-Bis(trifluoromethyl)benzyl alcohol 1-[2,5-BIS(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL (S)-1-[3,5-Bis(trifluoromethyl)phenyl]ethan-1-ol (R)-1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)ETHAN-1-OL

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