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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434683Generated: November 1, 2026

Tetrahydrofuran → 4-(2-bromo-acetyl)-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide

https://huagongshe.com/reaction/1434683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-Acetyl-n-(thiazol-2-yl)benzenesulfonamideHCID 21082529—
ReactantPyridiniumtribromideHCID 21124087—
SolventWaterHCID 962—
Product4-(2-bromo-acetyl)-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamideHCID 86611697—

Reaction Steps

To a solution of 4-acetyl-N-thiazol-2-yl-benzenesulfonamide (10 mmol) in THF (50 mL) was added pyridinium tribromide (10 mmol), and the mixture was stirred for 4 h. The reaction mixture was diluted with water (30 mL) and the resulting mixture was extracted with ethyl acetate. The organic phase was washed with brine, dried over MgSO4, and concentrated in vacuo. The crude product was purified by column chromatography to give 4-(2-bromo-acetyl)-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide (8.2 mmol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615569B2
Source datasetuspto-grants-2009_11
ORD IDord-182a8cebbf694424bd1e4f6844073fed
Source noteuspto-grants-2009_11