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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589457Generated: November 3, 2026

Ethanol → 2-(4-Fluorophenyl)-2-methylbutyl alcohol

https://huagongshe.com/reaction/1589457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
Reactant2-(4-Fluorophenyl)-2-methylbutanoic acidHCID 13711781—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Fluorophenyl)-2-methylbutyl alcoholHCID 1558265093.3%

Reaction Steps

A solution of 3.0 g of 2-(4-fluorophenyl)-2-methylbutyric acid in 10 ml of tetrahydrofuran was added dropwise to a mixture of 20 ml of tetrahydrofuran and 0.5 g of lithium aluminum hydride at 40° C. The temperature was then elevated and the mixture was refluxed for 30 minutes. The mixture was cooled to room temperature and ethanol was added dropwise to the mixture to decompose excessive lithium aluminum hydride. Then, water was added to the mixture to complete the decomposition. The formed precipitate was removed by filtration and tetrahydrofuran was removed from the filtrate by distillation under reduced pressure. The residue was extracted with benzene, and the benzene extract was washed with water direct, over Na2SO4, and evaporated under reduced pressure to give 2.6 g of 2-(4-fluorophenyl)-2-methylbutyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04570005
Source datasetuspto-grants-1986_02
ORD IDord-a9ca438ecc204a3796574b6cf746c659
Source noteuspto-grants-1986_02