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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842336Generated: October 31, 2026

Hydrochloric Acid → 1-Phenylethanol, (S)-

https://huagongshe.com/reaction/842336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetophenoneHCID 7410—
ReactantPotassium HydroxideHCID 14797—
SolventIsopropanolHCID 3776—
Product1-Phenylethanol, (S)-HCID 44313584%

Reaction Steps

The catalyst solution was added to a degassed 0.1M solution of KOH in 2-propanol, followed by a solution of acetophenone in 2-propanol. The mixture was stirred at ambient temperature under nitrogen for 2 h, then worked up by neutralising with dilute hydrochloric acid and concentrating by vacuum distillation. The residue was diluted with ethyl acetate and washed with an equal volume of saturated aqueous sodium chloride. The organic layer was separated, dried over magnesium sulphate, separated from the solid and freed of solvent to give crude (S)-1-phenylethanol (1.76 g). Yield 84%, ee 89%. The turnover number, integrated over 1 h, was 324 h−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372931B1
Source datasetuspto-grants-2002_04
ORD IDord-c2b167fe93c4428aa6d0eab54b603eca
Source noteuspto-grants-2002_04