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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111592Generated: October 29, 2026

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

https://huagongshe.com/reaction/1111592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant5-Bromothiazol-2-yl IsocyanateHCID 23062264—
Reactant2-beta-ChloroethylaminoacetaldehydeHCID 54332049—
SolventWater ethanolHCID 19096565—
Product2-[1-beta-Chloroethyl-3-(5-bromothiazol-2-yl)ureido]acetaldehydeHCID 54185255—

Reaction Steps

5-Bromothiazol-2-yl isocyanate dimer (17.0 grams), benzene (70 ml) and the dimethyl acetal of 2-β-chloroethylaminoacetaldehyde (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-β-chloroethyl-3-(5-bromothiazol-2-yl)ureido]acetaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04118390
Source datasetuspto-grants-1978_10
ORD IDord-e9d1dbcfe0cb4b728f59227f01ab5eca
Source noteuspto-grants-1978_10