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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54250Generated: October 30, 2026

Aluminium lithium hydride → 2-(4-Chlorophenyl)-2,2-difluoroethanol

https://huagongshe.com/reaction/54250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl 2-(4-Chlorophenyl)-2,2-difluoroacetateHCID 21468011—
SolventDiethyl EtherHCID 3283—
Product2-(4-Chlorophenyl)-2,2-difluoroethanolHCID 23237844—

Reaction Conditions

Temperature25 °C

Reaction Steps

Lithium aluminum hydride, 2.4 grams (0.063 mole), is placed in a reaction vessel, and 200 mL of diethyl ether is added dropwise with stirring. To this is added dropwise a solution of 22.8 grams (0.097 mole) of ethyl 4-chlorophenyldifluoroacetate (prepared by methods taught by W. J. Middleton et al., J. Org. Chem., (1980), 45, 2883-2887) in 100 mL of diethyl ether, while maintaining the reaction mixture temperature at about 25° C. Upon completion of addition, the reaction mixture is stirred at ambient temperature for about 36 hours. The reaction is then quenched by the careful dropwise addition of an aqueous solution of 10% sodium hydroxide. The reaction mixture is slowly made acidic with aqueous 2N hydrochloric acid and then is diluted with 200 mL of water. The organic layer is separated, and the aqueous layer is washed with two 300 mL portions of diethyl ether. The organic layer and the diethyl ether washes are combined and washed with one 250 mL portion of an aqueous solution saturated with sodium chloride. The organic layer is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure, yielding 2,2-difluoro-2-(4-chlorophenyl)ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622954
Source datasetuspto-grants-1997_04
ORD IDord-70bad8e5400b4f1ea01fe9649e17ad86
Source noteuspto-grants-1997_04