HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzophenone → N'-(Diphenylmethylene)-4-methylbenzenesulfonohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | P-Toluenesulfonylhydrazide | HCID 15303 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N'-(Diphenylmethylene)-4-methylbenzenesulfonohydrazide | HCID 274531 | — |
Reaction Steps
Benzophenone (15.0 parts, 0.082M ex Fluka) was stirred at reflux with p-toluene sulphonylhydrazine (15.33 parts, 0.082M ex Aldrich) in ethanol (125 ml) for 10 hours. Gradually a pale yellow solution formed from which the hydrazone gradually precipitated. After cooling to 20° C., diethylether (20 ml) was added and the hydrazone filtered and washed with ether. The hydrazone was obtained as a white powder (24.0 parts; 83% theory) mp 184°-6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05880188 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-058e646ba9944325b3e2a08806819c7b |
| Source note | uspto-grants-1999_03 |