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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4353Generated: October 25, 2026

Sodium borohydride → 1-Phenyl-1-[4-(4-pyridyl)-2-thiazolyl]methanol

https://huagongshe.com/reaction/4353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-Phenyl-1-[4-(4-pyridyl)-2-thiazolyl]methanoneHCID 14096958—
SolventMethanolHCID 887—
Product1-Phenyl-1-[4-(4-pyridyl)-2-thiazolyl]methanolHCID 1409695945%

Reaction Steps

To a solution of 1-phenyl-1-[4-(4-pyridyl)-2-thiazolyl]methanone (675 g, 0.0025 mol) in methanol (40 mL) was added sodium borohydride (300 mg, 0.0079 mol) in portions and the mixture allowed to stir at room temperature for one hour. The reaction mixture was concentrated, diluted with water, and extracted with ether (3×25 mL). The combined extracts were washed with brine, dried over magnesium sulfate, concentrated, and chromatographed. Recrystallization from hexane/ethyl acetate afforded 1-phenyl-1-[4-(4-pyridyl)-2-thiazolyl]methanol (300 mg, 45%). mp. 146°-147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04725606
Source datasetuspto-grants-1988_02
ORD IDord-e29bb60d5a354d0d869838cdbf5e9016
Source noteuspto-grants-1988_02