HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → N-(1,2,3-Thiadiazol-5-yl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(1,2,3-Thiadiazol-5-yl)benzamide | HCID 319747 | 36.6% |
Reaction Steps
To a stirred solution of benzoylisothiocyanate (50.6 g., 310 mmoles) in commercial anhydrous ether (400 ml.), maintained at 0° and in a nitrogen atmosphere, was added dropwise with vigorous stirring, 0.685 N ethereal diazomethane (453 ml., 310 mmoles). When the addition was completed, the mixture was stirred for 1 hour at 0°, the solid was collected by filtration and dried in vacuo. The melting point of the crude material (23.3 g.) thus obtained was observed somewhere in the region 232° to 257°. Goerdler reported M.p. 267° for the pure material. A small second crop (2.1 g.) was obtained by evaporation of the mother liquor in vacuo. The total yield was therefore 40%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03946000 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-11587bd8483a4699b52af6e688f52bb3 |
| Source note | uspto-grants-1976_03 |