HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-[4-(Diphenylmethylidene)piperidin-1-yl]butan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | N-[4-(4-diphenylmethylene-1-piperidyl)butyl]phthalimide | HCID 15096000 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[4-(Diphenylmethylidene)piperidin-1-yl]butan-1-amine | HCID 15616549 | 123.2% |
Reaction Steps
The obtained phthalimide compound (13.7 g) and hydrazine monohydrate (2.5 g) are added to ethanol (34 ml) and the mixture is refluxed with stirring for 2 hours. After cooling, a small amount of water is added to the reaction mixture and the solvent is distilled off under reduced pressure. Chloroform (200 ml) is added to the residue and the insoluble substances are filtered off and washed twice with chloroform (each 50 ml). The filtrate and the washings are combined together, washed with water, dried over anhydrous magnesium sulfate and concentrated to give the desired compound (12 g). Mass spectrum m/z: 320 (M+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04965266 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-f329b6ed778d4d788dc14baadbe47f5b |
| Source note | uspto-grants-1990_10 |