HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → 2-Cyclohexyl-5-isocyanato-1,3,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 5-Cyclohexyl-1,3,4-thiadiazol-2-amine | HCID 732629 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Cyclohexyl-5-isocyanato-1,3,4-thiadiazole | HCID 53924444 | — |
Reaction Steps
A saturated solution of phosgene in ethyl acetate (500 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer. 5-Cyclohexyl-2-amino-1,3,4-thiadiazole (6 grams) is added to the reaction vessel, and the resulting mixture is stirred and heated at reflux for a period of about 4 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 from a dimethyl formamide-water mixture to yield the desired product 5-cyclohexyl-1,3,4-thiadiazol-2-yl isocyanate dimer having a melting point of 237° to 239° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04043795 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-207b6eafd0b3432d89f710d45bb1b528 |
| Source note | uspto-grants-1977_08 |