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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520264Generated: October 26, 2026

Ammonium Chloride → 2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethan-1-ol

https://huagongshe.com/reaction/520264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2,2,2-Trifluoro-4'-(trifluoromethyl)acetophenoneHCID 144683—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethan-1-olHCID 11390886105.1%

Reaction Steps

In a 50 mL two-neck flask, 2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethanone (2.0 g, 8.3 mmol) was dissolved in methanol (8 mL) and sodium borohydride (0.31 g, 8.3 mmol) was added carefully in portions with ice-bath cooling. The resultant colourless solution was stirred at RT for 2 hours and monitored by TLC. Upon the disappearance of all starting material, 5 mL of an aqueous saturated NH4Cl solution was slowly added to the reaction mixture with additional stirring for 10 min. The later was extracted 3 times with 20 mL of EtOAc and the organic fractions were combined and washed with 10 mL of brine, dried over Na2SO4, and filtered. The solvent was removed under reduced pressure to give 2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethanol (2.13 g, quantitative) as a colourless oil which was used with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09326513B2
Source datasetuspto-grants-2016_05
ORD IDord-e683e4134cdc44cf945f314276bb5602
Source noteuspto-grants-2016_05