Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488177Generated: October 30, 2026

4-Hydroxybenzaldehyde → HCID 22860522, compound

https://huagongshe.com/reaction/488177

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant(αR)-4-Methyl-α-phenylbenzeneethanamineHCID 10138221—
SolventEthanolHCID 702—
ProductHCID 22860522HCID 2286052264.5%

Reaction Steps

21.13 g (0.1 mole) of (R)-(-)-α-phenyl-β-p-tolylethylamine (optical purity: 100%) and 12.82 g (0.105 mole) of p-hydroxybenzaldehyde were dissolved in 750 ml of ethyl alcohol. The reaction solution thus obtained was stirred at room temperature for 3 hours, and then stirred under reflux for 1 hour. Thereafter, the reaction solution was admixed at room temperature with 1.89 g (0.05 mole) of sodium borohydride, stirred for 3 hours, and then stirred under reflux for 1 hour. The reaction mixture was admixed with 75 ml of a 10% hydrochloric acid, and then concentrated under reduced pressure to give a crude (R)-(+)-N-p-hydroxybenzyl-α-phenyl-β-p-tolylethylamine·HCl salt, which was thereafter neutralized with an aqueous sodium hydroxide solution. The resultant solution was concentrated under reduced pressure to obtain the crystals, which were then recrystallized from ethyl alcohol, so that 20.47 g of (R)-(+)-N-p-hydroxybenzyl-α-phenyl-β-p-tolylethylamine were obtained as colorless crystals. Yield: 64.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298660
Source datasetuspto-grants-1994_03
ORD IDord-d829edc27d1f44b6a001e63fc7df375e
Source noteuspto-grants-1994_03