HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetyl chloride → N'-t-butyl-N-benzoyl-N'-phenylacetylhydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N'-tert-butylbenzohydrazide | HCID 299436 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N'-t-butyl-N-benzoyl-N'-phenylacetylhydrazine | HCID 15451997 | 90% |
Reaction Steps
N'-t-butyl-N-benzoylhydrazine (2 g) was stirred in toluene (35 ml) and 50% aqueous sodium hydroxide (1 g) at 5° C. Phenylacetylchloride (1.5 g) was added slowly, dropwise to the reaction mixture, warmed to room temperature and stirred 1 hour. The reaction mixture was diluted with hexane (50 ml) and filtered off to yield a solid product. The filter cake was washed with hexane and water and allowed to air dry. The white solid product obtained in 90% yield melted at 167-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06013836 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-b2e053bcf9aa4099b5337f99b8275cba |
| Source note | uspto-grants-2000_01 |