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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909435Generated: October 30, 2026

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

https://huagongshe.com/reaction/1909435

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-chlorophenyl)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 1 hour. The reaction mixture is quenched with saturated aqueous ammonium chloride solution (100 ml) and extracted with dichloromethane (2×150 ml). The combined organic extracts are dried over anhydrous magnesium sulfate, filtered and evaporated to dryness to give 1-[2-(4-chlorophenyl)thiazol-5-yl]ethanol (4.88 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598365B2
Source datasetuspto-grants-2013_12
ORD IDord-22bf957ffe1b41f3b3882d53d0da55d7
Source noteuspto-grants-2013_12