Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862943Generated: November 1, 2026

Phosgene → 5-Cyclobutyl-1,3,4-thiadiazol-2-yl isocyanate

https://huagongshe.com/reaction/1862943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
Reactant5-Cyclobutyl-1,3,4-thiadiazol-2-amineHCID 16450167—
SolventEthyl AcetateHCID 8857—
Product5-Cyclobutyl-1,3,4-thiadiazol-2-yl isocyanateHCID 54345741—

Reaction Steps

A saturated solution of phosgene in ethyl acetate (100 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer. A slurry of 5-cyclobutyl-2-amino-1,3,4-thiadiazole (45 grams) in ethyl acetate (300 ml) is added to the reaction vessel and the resulting mixture is stirred for a period of about 16 hours, resulting in the formation of a precipitate. The reaction mixture is then purged with nitrogen gas to remove unreacted phosgene. The purged mixture is then filtered to recover the precipitate. The precipitate is then recrystallized to yield the desired product 5-cyclobutyl-1,3,4-thiadiazol-2-yl isocyanate dimer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04167407
Source datasetuspto-grants-1979_09
ORD IDord-5025fa33374a4ad0a65aa4a2e65a2e59
Source noteuspto-grants-1979_09