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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2828Generated: October 26, 2026

2-Acetylbenzofuran → 1-(2-Benzofuranyl)-1-(4-methyl-5-thiazolyl)ethanol

https://huagongshe.com/reaction/2828

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AcetylbenzofuranHCID 15435—
Reactant4-Methyl-2-trimethylsilylthiazoleHCID 11658354—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product1-(2-Benzofuranyl)-1-(4-methyl-5-thiazolyl)ethanolHCID 18936360—

Reaction Steps

n-Butyllithium (2.5M solution in hexane, 1 equivalent) was added dropwise to a solution of 4-methyl-2-trimethylsilylthiazole (1 equivalent) in dry diethyl ether at -70° C. under an atmosphere of dry nitrogen. After 30 minutes, 2-acetylbenzofuran (1 equivalent) in diethyl ether was added. After 1 hour the mixture was allowed to warm to room temperature and was then quenched by the addition of saturated aqueous sodium hydrogen carbonate. Work up in the normal fashion and column chromatography on silica gel then afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731335
Source datasetuspto-grants-1998_03
ORD IDord-9c11173c9d7a4647bd65210ad622b55b
Source noteuspto-grants-1998_03