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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051426Generated: November 2, 2026

Bromine → N-(4-bromo-2-methylthiazol-5-yl)acetamide

https://huagongshe.com/reaction/1051426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantN-(2-Methylthiazol-5-yl)acetamideHCID 73554716—
SolventChloroformHCID 6212—
SolventSodium BisulfiteHCID 23665763—
ProductN-(4-bromo-2-methylthiazol-5-yl)acetamideHCID 8671555967%

Reaction Steps

To a solution of N-(2-methylthiazol-5-yl)acetamide (0.4 g, 2.6 mmol) in CHCl3 (30 mL) was added Br2 (0.15 mL, 2.8 mmol), then the solution was stirred at room temperature for 12 h to give a brown solution. The reaction mixture was diluted with saturated NaHSO3 solution. The aqueous layer was extracted with DCM (3×30 mL). The combined organic layers were dried with Na2SO4, filtered and concentrated to afford a yellow solid. The resulting mixture was deposited onto silica gel and loaded onto a silica gel column and eluted with PE/EA(1:1) to give the title compound (400 mg, yield 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388180B2
Source datasetuspto-grants-2016_07
ORD IDord-432fd5a06d8249868afbdf458b1a3e7c
Source noteuspto-grants-2016_07