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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704838Generated: October 30, 2026

Benzaldehyde → N-benzyl-1-(3,4-dimethoxyphenyl)ethanamine

https://huagongshe.com/reaction/704838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant1-(3,4-Dimethoxyphenyl)ethan-1-amineHCID 3159243—
ReactantSodium borohydrideHCID 4311764—
CatalystPyridineHCID 1049—
SolventMethanolHCID 887—
ProductN-benzyl-1-(3,4-dimethoxyphenyl)ethanamineHCID 2756621100%

Reaction Steps

A mixture containing 18.1 g of 1-amino-1-(3,4-dimethoxyphenyl)-ethane (J. Chem. Soc. 1963, 4289), 10,6 g of benzaldehyde and 1 drop of pyridine in 100 ml of methanol is let stand at 20° C. for 2 days, then 3.8 g of sodium borohydride are added during 30 minutes and stirred for additional 3 hours. After evaporation of the solvent, the residue is diluted with water, extracted with chloroform, the organic phase is dried and evaporated to give 27.1 g of the crude title compound, which can directly be used in the process described in Example 6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988730
Source datasetuspto-grants-1991_01
ORD IDord-410bde7194ba4142b2429f990e3a0d04
Source noteuspto-grants-1991_01