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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849974Generated: October 31, 2026

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

https://huagongshe.com/reaction/1849974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-(4-Chlorophenyl)-1,3-thiazole-5-carbaldehydeHCID 45036822—
SolventMethanolHCID 887—
Product[2-(4-Chlorophenyl)thiazol-5-yl]methanolHCID 5956241698.3%

Reaction Steps

To a suspension of 2-(4-chlorophenyl)thiazole-5-carbaldehyde (3.26 g, 14.6 mmol) in methanol (50 ml) is added the sodium borohydride (568 mg, 15 mmol) portionwise at room temperature. The reaction mixture is stirred at room temperature for 2 h. The reaction mixture is quenched with 50 ml of an aqueous saturated solution of ammonium chloride, extracted with dichloromethane (2×100 ml). The combined organic extracts are dried with magnesium sulphate, filtered and evaporated to dryness to give [2-(4-chlorophenyl)thiazol-5-yl]methanol (3.24 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08956999B2
Source datasetuspto-grants-2015_02
ORD IDord-31e7fe97978645ac95802f4f75d84ec1
Source noteuspto-grants-2015_02