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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105619Generated: October 25, 2026

Water → N-{2-(4-{(E)-2-Carbomethoxyethenyl}phenyl)-1-methylethyl}2-hydroxy-2-phenylethanamine

https://huagongshe.com/reaction/1105619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenylethanolamineHCID 1000—
Reactant4-{(E)-2-carbomethoxyethenyl}phenylpropan-2-oneHCID 19874532—
SolventBenzeneHCID 241—
ProductN-{2-(4-{(E)-2-Carbomethoxyethenyl}phenyl)-1-methylethyl}2-hydroxy-2-phenylethanamineHCID 20556102—

Reaction Steps

A mixture of 4-(E)-(2-carbomethoxyethenyl)phenylpropan-2-one (2.18 g) and 2-hydroxy-2-phenylethanamine (1.37 g) was refluxed in benzene under a Dean and Stark apparatus until the theoretical amount of water had been collected. The solvent was evaporated, methanol added, and sodium borohydride (1.0 g) added portionwise at room temperature. The solution was left to stir for 0.5 h, and solvent removed. Water was added, the mixture extracted with ether and the combined ether layers dried (MgSO4). Removal of the solvent gave the title compound, isolated as a 1:1 mixture of diastereoisomers, as the hemi-fumarate hemihydrate mp 99°-100.5° (ethyl acetate). τ (DMSO) 8.95 (3H, d, J=6 Hz), 6.4-7.5 (5H, m), 6.31 (3H, s), 5.2-4.9 (1H, m), 3.45 (1H, d, J=16 Hz+2H, s), 2.15-2.9 (10H, m), 1.6 (4H, s, disappears with D2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04309443
Source datasetuspto-grants-1982_01
ORD IDord-757606701a6a4d1dadc6057e92c258b7
Source noteuspto-grants-1982_01