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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849964Generated: October 31, 2026

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

https://huagongshe.com/reaction/1849964

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 5956247596.8%

Reaction Steps

To a stirred solution of 1-[2-(4-chlorophenyl)thiazol-5-yl]ethanone (2.38 g, 10 mmol) in methanol (20 ml) at 0° C. is added sodium borohydride (379 mg, 10.5 mmol) in one portion. The resultant solution is allowed to warm to room temperature, and is then stirred at room temperature for 3 hours. The reaction is quenched with saturated aqueous ammonium chloride solution (200 ml) and extracted with chloroform (200 ml). The organic layer is dried over anhydrous magnesium sulfate and concentrated in vacuuo to give desired product as a brown solid (2.32 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08956999B2
Source datasetuspto-grants-2015_02
ORD IDord-0ba5604d72534a50bf49f6905b656d5f
Source noteuspto-grants-2015_02