HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-Acetyl-4-(2,4-dichlorobenzoyl)piperidine oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 4-(2,4-dichlorobenzoyl)-N-acetylpiperidine | HCID 13076387 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Acetyl-4-(2,4-dichlorobenzoyl)piperidine oxime | HCID 86027872 | 31.1% |
Reaction Steps
A mixture of 13.0 g of 4-(2,4-dichlorobenzoyl)-N-acetylpiperidine, 6.8 g of hydroxylamine hydrochloride, 13.5 g of ammonium acetate, 127 ml of ethanol and 43 ml of water was stirred and heated at 130° for 24 hrs. The reaction mixture was evaporated and 1.3 l of water was added to the residue. The water was decanted from the oil and the oil was dissolved in about 150 ml dichloromethane. After washing with about 150 ml of water, drying over anhydrous magnesium sulfate and evaporating the solvent, an oil was obtained, which after crystallization from methanol/ether gave 4.25 g (31.1%) of product, mp 167°-168°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04408054 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-9f1ea326aa234f18b5c63d4e03ff2d90 |
| Source note | uspto-grants-1983_10 |