HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → N'-t-butyl-N-benzoyl-N'-(beta-trifluoromethylcrotonyl)hydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | N'-tert-butylbenzohydrazide | HCID 299436 | — |
| Reactant | 4,4,4-Trifluoro-3-methyl-2-butenoic acid | HCID 5708835 | — |
| Reactant | beta-Trifluoromethylcrotonyl chloride | HCID 86745869 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N'-t-butyl-N-benzoyl-N'-(beta-trifluoromethylcrotonyl)hydrazine | HCID 70294050 | — |
Reaction Steps
N'-t-butyl-N-benzoylhydrazine (1.0 g,) in 2 ml toluene was added dropwise to a solution of beta-trifluoromethylcrotonyl chloride (prepared by addition of oxalyl chloride (1.3 g) to a solution of 1.5 g beta-trifluoromethylcrotonic acid in 5 ml toluene at 23° C.). After 30 min. at 23° C., the reaction mixture was partitioned between saturated aqueous sodium bicarbonate (20 ml) and ether (20 ml). The ether layer was evaporated under reduced pressure to about 10 ml and the excess hydrazine was removed by filtration. The filtrate was evaporated to give N'-t-butyl-N-benzoyl-N'-(beta-trifluoromethylcrotonyl)hydrazine as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06013836 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-a0ec4bd5c3bd41b99ae4fbc230312fe8 |
| Source note | uspto-grants-2000_01 |