Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065474Generated: October 29, 2026

3,3-Diphenylacrolein → HCID 13065282, compound

https://huagongshe.com/reaction/1065474

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-DiphenylacroleinHCID 71027—
Reactant1-[4-(Benzyloxy)phenyl]propan-2-amineHCID 134616—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 13065282HCID 13065282—

Reaction Steps

The starting material is prepared as follows: The solution of 12 g of dl-p-benzyloxyamphetamine, and 10.4 g of β-phenyl-cinnamaldehyde in 300 ml of absolute ethanol is treated dropwse with the solution of 3 g of sodium borohydride in 6.7 ml of water while stirring. It is refluxed for 18 hours, concentrated to remove most of the ethanol and diluted with water. The mixture is extracted with ethyl acetate and the organic layer washed with brine, dried and evaporated, to yield the dl-1-(p-benzyloxyphenyl)-2-(3,3-diphenylallylamino)-propane; its maleate melts at 177°-178°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04329367
Source datasetuspto-grants-1982_05
ORD IDord-dec3d6f7cac04e4aad5cf5116fca34f3
Source noteuspto-grants-1982_05