HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → 3-(1-Diphenylmethylpiperidine-4-yl)-propylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 2-[3-(1-Diphenylmethylpiperidine-4-yl)-propyl]-isoindol-1,3-dione | HCID 18425726 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(1-Diphenylmethylpiperidine-4-yl)-propylamine | HCID 18425732 | — |
Reaction Steps
12.8 g (29.2 mmol) 2-[3-(1-diphenylmethylpiperidine-4-yl)-propyl]-isoindol-1,3-dione are suspended in 110 ml ethanol and added to 2.2 ml (58.4 mmol) hydrazine hydrate and heated to boiling for three hours. After cooling, the mixture is concentrated under vacuum. The residue is dispersed between 300 ml dichloromethane and 50 ml 10% sodium hydroxide solution. The aqueous phase is extracted twice, each with 200 ml dichloromethane. The combined organic phases are washed twice, each with 20 ml water, and dried over sodium sulfate. The solvent is removed under vacuum and the residue is processed fruther without additional purification. Yield 7.3 g (81%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06451816B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-0b661ec4c00b4166a7987263b5746957 |
| Source note | uspto-grants-2002_09 |