HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → N'-t-butyl-N-benzoyl-N'-benzenesulfonylhydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | N'-tert-butylbenzohydrazide | HCID 299436 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N'-t-butyl-N-benzoyl-N'-benzenesulfonylhydrazine | HCID 14623256 | — |
Reaction Steps
N-benzoyl-N'-t-butyl hydrazine (0.8 g) was stirred in pyridine (2 ml) at room temperature. Benzenesulfonyl chloride (0.8 g) was added slowly dropwise, stirred about 1 hour, diluted with diethyl ether (10 ml) and washed several times with a 10% HCl solution and then water. The organic layer was dried over magnesium sulfate. The mixture was filtered and the solvent rotavapped off to afford a white solid in good yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06013836 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-b475a802fb5147c094cf205d0b08e16c |
| Source note | uspto-grants-2000_01 |