HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 13194658, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-chloro-N-(propan-2-ylideneamino)benzamide | HCID 351632 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13194658 | HCID 13194658 | 82% |
Reaction Steps
10.5 g of 1-p-chlorobenzoyl-2-isopropylidene hydrazine, 5.3 g of triethylamine and 100 ml of tetrahydrofuran were placed in a 200 ml round-bottom flask, and while stirring with ice-water cooling, 3.9 of acetylchloride was dropped gradually. After dropping, the mixture was heated at reflux for one hour so as to complete the reaction. The reaction mixture was cooled to room temperature and the separated salts were filtered off, and then the filtrate was concentrated to obtain yellow brown crystals, which were then recrystallized from a mixed solvent of hexane/acetone to yield 10.4 g (82%) of yellow crystalline 1-p-chlorobenzoyl-1-acetyl-2-isopropylidene hydrazine having a melting point of 73°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04547524 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-62146071440d4092990a46123d4b731d |
| Source note | uspto-grants-1985_10 |