HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-[(2,4-Dichlorophenyl)(hydroxyimino)methyl]-1-piperidinecarboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 4-(2,4-Dichlorobenzoyl)piperidine-1-carbaldehyde | HCID 13450895 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[(2,4-Dichlorophenyl)(hydroxyimino)methyl]-1-piperidinecarboxaldehyde | HCID 88643199 | 14.2% |
Reaction Steps
A mixture of 105 g of 4-(2,4-dichlorobenzoyl)-1-formylpiperidine, 70 g of hydroxylamine hydrochloride, 135.0 g of ammonium acetate, 1.05 l of ethanol and 350 ml of water was stirred and heated at 130° for 40 hrs. The reaction mixture was evaporated and 2 l of water was added to the residue. The water was decanted from the oil and oil was washed two times with 500 ml water and then dissolved in about 400 ml dichloromethane. The insoluble material was collected. The dichloromethane extract was washed twice with 600 ml of water and the organic extract was evaporated. Trituration with diisopropyl ether and crystallization from acetone/ether gave 15.6 g (14.2%) of product, mp, 149°-150°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04528376 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-2429b578ad21457bad7a2cbb428b98c0 |
| Source note | uspto-grants-1985_07 |