Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764463Generated: October 31, 2026

Benzene → 2-[1-Chloromethyl-3-(5-bromothiazol-2-yl)ureido]acetaldehyde

https://huagongshe.com/reaction/1764463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant2-ChloromethylaminoacetaldehydeHCID 20392716—
Reactant5-Bromothiazol-2-yl IsocyanateHCID 23062264—
SolventWater ethanolHCID 19096565—
Product2-[1-Chloromethyl-3-(5-bromothiazol-2-yl)ureido]acetaldehydeHCID 22768499—

Reaction Steps

5-Bromothiazol-2-yl isocyanate dimer (17.0 grams), benzene (70 ml) and the dimethyl acetal of 2-chloromethylaminoacetaldehyde (13.5 grams) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is then stirred at room temperature for a period of about 1 hour. After this time the reaction mixture is filtered, and the filtrate is stripped of solvent under reduced pressure, leaving an oil. This oil is dissolved in an ethanol-water mixture, and the solution is filtered. The filtrate is then stripped of solvents under vacuum to yield the desired product the dimethyl acetal of 2-[1-chloromethyl-3-(5-bromothiazol-2-yl)ureido]acetaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116969
Source datasetuspto-grants-1978_09
ORD IDord-ba9923d7a98843c6a812dfde863c565e
Source noteuspto-grants-1978_09