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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942642Generated: November 3, 2026

Bromine → 5-Bromo-2-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazole

https://huagongshe.com/reaction/1942642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
Reactant2-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazoleHCID 58494140—
SolventAcetic AcidHCID 176—
Product5-Bromo-2-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazoleHCID 58494106—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 2-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazole (D70) (1.5 g) and sodium acetate (0.970 g) in acetic acid (10 mL) stirred at room temperature was added a solution of Br2 (0.31 ml) in acetic acid (1 mL) dropwise during 30 min. The reaction mixture was stirred at 20° C. until start material was consumed completely. The reaction mixture was basified with 2M NaOH. The resulting solution was diluted with ethyl acetate. The mixture was washed with brine. The organic phase was dried over anhydrous sodium sulphate and evaporated in vacuo. The crude product was purified by column chromatography to give 5-bromo-2-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazole (D71) (1.2 g). MS (ES): C12H11BrClNOS requires 332. found 333.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389508B2
Source datasetuspto-grants-2013_03
ORD IDord-f9a4cab9c1d84b0781954e4addebd7ec
Source noteuspto-grants-2013_03