Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426305Generated: October 25, 2026

Water → N-(5-Bromothiazol-2-yl)-N-methylacetamide

https://huagongshe.com/reaction/2426305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Acetamido-5-bromo-1,3-thiazoleHCID 350260—
SolventAcetoneHCID 180—
ProductN-(5-Bromothiazol-2-yl)-N-methylacetamideHCID 6714780336.8%

Reaction Steps

1.9 g (14 mmol) of potassium carbonate and 3.94 ml (63.3 mmol) of methyl iodide are added to a solution of 2.8 g (12.7 mmol) of N-(5-bromothiazol-2-yl)acetamide in 50 ml of acetone. The reaction medium is refluxed for 3 hours. After addition of water, the reaction medium is extracted with ethyl acetate. The organic phase is washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with a 7/3 heptane/ethyl acetate mixture. 1.1 g (36%) of N-(5-Bromothiazol-2-yl)-N-methylacetamide are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968560B2
Source datasetuspto-grants-2011_06
ORD IDord-be10c38530f643d498acdaac86883439
Source noteuspto-grants-2011_06