Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918151Generated: October 26, 2026

Hydrochloric Acid → 3-(2-Fluoro-4-biphenylyl)-1-butanol

https://huagongshe.com/reaction/918151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3-(3-Fluoro-4-phenylphenyl)butanoic acidHCID 21523267—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Fluoro-4-biphenylyl)-1-butanolHCID 21523265—

Reaction Steps

A solution of 25.83 gm (0.10 mol) of 3-(2-fluoro-4-biphenylyl)-butyric acid in 100 ml of absolute tertrahydrofuran was added dropwise at room temperature to a stirred suspension of 2.85 gm (0.075 mol) of lithium aluminum hydride in 100 ml of absolute tetrahydrofuran, the resulting mixture was stirred for 60 minutes more at room temperature and for 30 minutes at 30°-35°C, and then ethyl acetate was added dropwise until no more exothermic reaction occurred. The reaction mixture was then stirred for 15 minutes at room temperature, and thereafter first 50 ml of water and then aqueous 5% hydrochloric acid were added dropwise, accompanied by exterior cooling with ice water, until the precipitate first formed dissolved. The solution was stirred into 2 liters of water, extracted exhaustively with ether, and the combined ether extracts were washed successively with water, saturated aqueous sodium bicarbonate solution and again with water, dried over sodium sulfate, filtered, and evaporated. 18.0 gm (74% of theory) of colorless 3-(2-fluoro-4-biphenylyl)-1-butanol of the formula ##EQU25## which had a melting point of 72°C after recrystallization from cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03969419
Source datasetuspto-grants-1976_07
ORD IDord-a742ebdeebee401bb76ba234c1808f8d
Source noteuspto-grants-1976_07