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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671470Generated: November 1, 2026

Hydrochloric Acid → (alphaS)-alpha-(Chloromethyl)-4-fluorobenzenemethanol

https://huagongshe.com/reaction/1671470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Chloro-4'-fluoroacetophenoneHCID 120248—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant(3aS)-1-methyl-3,3-diphenyl-hexahydropyrrolo(1,2-c)(1,3,2)oxazaboroleHCID 2734713—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product(alphaS)-alpha-(Chloromethyl)-4-fluorobenzenemethanolHCID 1001241599.3%

Reaction Steps

A borane-tetrahydrofuran complex (1.0 M solution in tetrahydrofuran, 60 ml, 60 mmol) was added dropwise over 15 min to a (S)—CBS solution ((S)-2-methyl-CBS-oxazaborolidine, 12 ml, 1.0 M solution in toluene) at −30° C., and the mixture was stirred for 15 min. A solution of 4-fluorophenacyl chloride (10.4 g, 60 mmol) in dichloromethane (16 ml) was added dropwise over 60 min keeping the temperature −32° C. to −28° C. After stirring for 1 hr, the solution was allowed to warm to room temperature, and methanol (20 ml) was added slowly and then 1 M hydrochloric acid (120 ml) was added dropwise over 10 min. The reaction mixture was filtered after stirring for 40 min, and the filtrate was extracted with ethyl acetate. The combined organic layer was washed successively with 1 M hydrochloric acid and brine, and dried over anhydrous sodium sulfate. The organic layer was concentrated to give 2-chloro-(1S)-1-(4-fluorophenyl)ethanol (10.4 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994315B2
Source datasetuspto-grants-2011_08
ORD IDord-44ae819884534358b92ca3de7036fcbe
Source noteuspto-grants-2011_08