HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → 5-Cycloheptyl-1,3,4-thiadiazol-2-yl isocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 5-Cycloheptyl-2-amino-1,3,4-thiadiazole | HCID 21447832 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Cycloheptyl-1,3,4-thiadiazol-2-yl isocyanate | HCID 21481918 | — |
Reaction Steps
A saturated solution of phosgene in ethyl acetate (100 ml) was charged into a glass reaction vessel equipped with a mechanical stirrer. A slurry of 5-cycloheptyl-2-amino-1,3,4-thiadiazole (45 grams) in ethyl acetate (300 ml) was added to the reaction vessel and the resulting mixture was stirred for a period of about 16 hours resulting in the formation of a precipitate. The reaction mixture was then purged with nitrogen gas to remove unreacted phosgene. The purged mixture was filtered to recover 48 grams of a white solid. This solid was recrystallized for dimethyl formamide to yield the desired product 5-cycloheptyl-1,3,4-thiadiazol-2-yl isocyanate dimer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04004912 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-f97b6f174a3a457b814425d0be9d6171 |
| Source note | uspto-grants-1977_01 |