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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phenylethanolamine | HCID 1000 | — |
| Reactant | 4-{(E)-2-carbomethoxyethenyl}phenylpropan-2-one | HCID 19874532 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-{2-(4-{(E)-2-Carbomethoxyethenyl}phenyl)-1-methylethyl}2-hydroxy-2-phenylethanamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04309443 |
|---|
| Source dataset | uspto-grants-1982_01 |
|---|
| ORD ID | ord-757606701a6a4d1dadc6057e92c258b7 |
|---|
| Source note | uspto-grants-1982_01 |
|---|