HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → N'-t-butyl-N-benzenesulfonyl-N'-benzoylhydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | N-(tert-butyl)benzohydrazide | HCID 1275961 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N'-t-butyl-N-benzenesulfonyl-N'-benzoylhydrazine | HCID 14623289 | — |
Reaction Steps
N'-t-butyl-N'-benzoylhydrazine (0.4 g) was stirred in pyridine (3 ml) at room temperature. Benzenesulfonyl chloride (0.5 g) was added slowly, dropwise and stirred for 2 hours, diluted with diethyl ether (20 ml) and washed several times with a 10% HCl solution and then water. The organic layer was dried over magnesium sulfate, 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 | US05424333 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-47782f9b5f06407a89236f994f00b2a5 |
| Source note | uspto-grants-1995_06 |