Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058854Generated: November 4, 2026

Ethyl chloroformate → ethyl N-(5-ethyl-7-chloro-4,5,6,7-tetrahydrobenzothiazol-2-yl)carbamate

https://huagongshe.com/reaction/2058854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant2-Amino-5-ethyl-7-chloro-4,5,6,7-tetrahydrobenzothiazoleHCID 20548470—
SolventPyridineHCID 1049—
Productethyl N-(5-ethyl-7-chloro-4,5,6,7-tetrahydrobenzothiazol-2-yl)carbamateHCID 20548458—

Reaction Steps

2-Amino-5-ethyl-7-chloro-4,5,6,7-tetrahydrobenzothiazole (0.10 mol) dissolved in pyridine (125 ml.) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and addition funnel. Ethyl chloroformate (0.12 mol) is then added dropwise to the reaction mixture with stirring and cooling. After the addition is completed the reaction mixture is allowed to warm to room temperature and stirring is continued for a period of about 1 hour. After this time the reaction mixture is poured into ice water to form a precipitate. The precipitate is recovered by filtration, is dried and recrystallized to yield the desired product ethyl N-(5-ethyl-7-chloro-4,5,6,7-tetrahydrobenzothiazol-2-yl)carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04319914
Source datasetuspto-grants-1982_03
ORD IDord-ed63c4b7168e4621a11447da5aa85552
Source noteuspto-grants-1982_03