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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828322Generated: October 31, 2026

N-bromobutanimide → HCID 11821667, compound

https://huagongshe.com/reaction/1828322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22066151HCID 22066151—
SolventChloroformHCID 6212—
ProductHCID 11821667HCID 11821667—

Reaction Steps

400 mg (2.1 mmol) of N-bromosuccinimide was added into 10 ml of anhydrous chloroform with 400 mg (2.1 mmol) of 5-methoxy-2-phenylthiazole under 0° C. condition and was stirred for 4 hours at a room temperature. After completion of reaction, the organic phase was extracted with ethyl acetate, and was dried with addition of magnesium sulfate. After removing the solvent, the product was developed with ethyl acetate:hexane=1:3 solvent on silica column to give 4-bromo-5-methoxy-2-phenylthiazole (Rf=0.50). The yield was 550 mg in weight and 97% in percentage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07057054B2
Source datasetuspto-grants-2006_06
ORD IDord-d31fa127692248f28b9ebd3d66c10841
Source noteuspto-grants-2006_06