HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → [2,3-bis(Acetyloxy)benzoyl]hydrazinecarboxylic acid, t-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl carbazate | HCID 70091 | — |
| Reactant | 3-(Chlorocarbonyl)-1,2-phenylene diacetate | HCID 15620412 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [2,3-bis(Acetyloxy)benzoyl]hydrazinecarboxylic acid, t-butyl ester | HCID 86742713 | — |
Reaction Steps
N-[(t-Butyloxy)carbonyl]hydrazine (12 g) and 10 g of triethylamine were dissolved in 200 ml of dichloromethane and, at 0° C., 24 g of 2,3-bis(acetyloxy)benzoyl chloride in 50 ml of dichloromethane was added dropwise with stirring (30 minutes). After continuous stirring for one hour, the reaction mixture was extracted with 200 ml of ice water, 50 ml of 1% sodium bicarbonate and 100 ml of 5% citric acid. The organic phase was then washed with 100 ml of water, dried over sodium sulfate, and the solvent distilled off. The remaining oil crystallized after stirring with hexane. The result was beige crystals, 26.3 g; melting point 117° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04801705 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-4adfd776424044dba590eaa0c1e1cf75 |
| Source note | uspto-grants-1989_01 |