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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710869Generated: November 1, 2026

Hydrochloric Acid → 1-[3,5-Bis(trifluoromethyl)phenyl]propan-1-ol

https://huagongshe.com/reaction/1710869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
Product1-[3,5-Bis(trifluoromethyl)phenyl]propan-1-olHCID 1023630949%

Reaction Steps

A solution of 3,5-bis(trifluoromethyl)benzaldehyde (300 mg, 1.24 mmol) in anhydrous tetrahydrofuran (3 mL) was added with ethylmagnesium bromide (1.00 M solution in anhydrous tetrahydrofuran, 1.86 mL, 1.86 mmol) with stirring on an ice bath, and the mixture was stirred at the same temperature for 30 minutes. The reaction mixture was added with 1 M hydrochloric acid on an ice bath (pH<7), and then the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1) to obtain 1-[3,5-bis(trifluoromethyl)phenyl]-1-propanol (165 mg, 49%) as colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790737B2
Source datasetuspto-grants-2010_09
ORD IDord-f16818a1d51a41ab96820854320e161e
Source noteuspto-grants-2010_09