Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559503Generated: October 29, 2026

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

https://huagongshe.com/reaction/559503

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 numberUS08063080B2
Source datasetuspto-grants-2011_11
ORD IDord-91b89a7ba15f48be93fa5a71156d8de9
Source noteuspto-grants-2011_11