HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzoyl chloride → 5-(4-Nitrobenzamido)-3-Trichloromethyl-1,2,4-Thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | 3-(Trichloromethyl)-1,2,4-thiadiazol-5-amine | HCID 602848 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(4-Nitrobenzamido)-3-Trichloromethyl-1,2,4-Thiadiazole | HCID 13041519 | 73.5% |
Reaction Steps
A solution of 10.9 g (0.05 mole) 5-amino-3-trichloromethyl-1,2,4-thiadiazole and 10.2 g (0.055 mole) 4-nitrobenzoyl chloride in 200 ml toluene was heated at reflux for 20 hours. Upon cooling to room temperature, the crude product precipitated from the reaction mixture and was isolated by filtration. After washing with hexane, 13.5 g (73% yield) of pure product was obtained; m.p. 214° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04343945 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-cf535115d4a34be684be0052ae84a514 |
| Source note | uspto-grants-1982_08 |