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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591012Generated: October 29, 2026

N-bromobutanimide → Methyl 2-(5-bromo-2-methyl-1,3-thiazol-4-yl)-2-(tert-butoxy)acetate

https://huagongshe.com/reaction/591012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-(tert-butoxy)-2-(2-methyl-1,3-thiazol-4-yl)acetateHCID 70819407—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(5-bromo-2-methyl-1,3-thiazol-4-yl)-2-(tert-butoxy)acetateHCID 70819398—

Reaction Conditions

Temperature70 °C

Reaction Steps

Under a nitrogen atmosphere, N-bromosuccinimide (39 mg, 0.22 mmol) was added to a solution of methyl 2-(tert-butoxy)-2-(2-methyl-1,3-thiazol-4-yl)acetate (15c) (50 mg, 0.21 mmol) in N,N-dimethylformamide (4 mL). The reaction mixture was warmed at 70° C. for 30 minutes then concentrated in vacuo. The residue was diluted with ethyl acetate (40 mL) and washed with water (2×20 mL), brine (20 mL), dried over sodium sulfate, filtered and evaporated under reduced pressure to give the desired product as a yellow oil without further purification (70 mg, 0.21 mmol, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-47fe65bfa4df4e749b86ed1184bd5ccd
Source noteuspto-grants-2016_01