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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41668Generated: October 30, 2026

Sodium borohydride → 1-[2-(4-Chlorophenyl)thiazol-5-yl]ethanol

https://huagongshe.com/reaction/41668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-[2-(4-Chlorophenyl)-1,3-thiazol-5-yl]-1-ethanoneHCID 7062288—
SolventMethanolHCID 887—
Product1-[2-(4-Chlorophenyl)thiazol-5-yl]ethanolHCID 5956247596.9%

Reaction Steps

To a suspension of 1-[2-(4-chloro-phenyl)-thiazol-5-yl]ethanone (5 g, 21 mmol) in methanol (100 ml) is added sodium borohydride (832 mg, 22 mmol) at room temperature. The reaction mixture is stirred at room temperature for 0.5 hour. The reaction mixture is quenched with 100 ml of an aqueous saturated solution of ammonium chloride, extracted with dichloromethane (2×150 ml). The combined organic extracts are dried over magnesium sulphate, filtered and evaporated to dryness to give 1-[2-(4-chloro-phenyl)-thiazol-5-yl]ethanol (4.88 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530667B2
Source datasetuspto-grants-2013_09
ORD IDord-9c642914da4d4470aa47031ae72f88b8
Source noteuspto-grants-2013_09