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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071268Generated: October 31, 2026

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

https://huagongshe.com/reaction/2071268

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 one 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 numberUS04046768
Source datasetuspto-grants-1977_09
ORD IDord-7efefc14b16a4ad79290f8dbfab67bd4
Source noteuspto-grants-1977_09