HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 20311665, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3,3-Diphenylacrolein | HCID 71027 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20311667 | HCID 20311667 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20311665 | HCID 20311665 | — |
Reaction Steps
The starting material is prepared as follows: The mixture of 12.1 g of dl-4-(2-pyridylmethoxy)-amphetamine, 400 ml of absolute ethanol and 10.4 g of β-phenylcinnamaldehyde is treated dropwise under stirring with the solution of 3.5 g of sodium borohydride in 10 ml of water. The whole is then stirred and refluxed overnight, concentrated and the concentrate diluted with water. It is extracted with ethyl acetate, the organic layer washed with saturated aqueous sodium chloride, dried and evaporated to yield the dl-1-[4-(2-pyridylmethoxy)-phenyl]-2-(3,3-diphenylallylamino)-propane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04110457 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-9a45554ec1bb46d288193e2b2cce42ec |
| Source note | uspto-grants-1978_08 |