HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112029Generated: November 4, 2026
3-(4-Hydroxyphenyl)propionic acid → N-[2-(2-ethoxyphenyl)ethyl]-3-(4-hydroxyphenyl)propanamide
https://huagongshe.com/reaction/2112029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(4-Hydroxyphenyl)propionic acid | HCID 10394 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Ethoxyphenethylamine | HCID 142362 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[2-(2-ethoxyphenyl)ethyl]-3-(4-hydroxyphenyl)propanamide | HCID 68873053 | 104.2% |
Reaction Steps
2-(2-Ethoxyphenyl)ethanamine (0.55 g, 3.33 mmol) and 3-(4-hydroxyphenyl)propanoic acid (0.50 g, 3.00 mmol) was dissolved in dimethyl formamide (5 ml) and cooled to 0° C. N-[(1H-1,2,3-benzotriazol-1-yloxy)(dimethylamino)methylene]-N-methylmethanaminium tetrafluoroborate (1.18 g, 3.66 mmol) and diisopropylethylamine (0.90 g, 7.0 mmol) were added and the solution was warmed to room temperature and stirred overnight. EtOAc (15 ml) was added and the organic phase was washed with two portions of sodium hydrogencarbonate (aq, 10 ml). The organic phase was dried (MgSO4) and EtOAc was removed by evaporation to give 0.98 gram of N-[2-(2-ethoxyphenyl)ethyl]-3-(4-hydroxyphenyl)propanamide (yield 93.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07521461B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-af8ff9fcbf7b4f3da9f3456e11896101 |
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| Source note | uspto-grants-2009_04 |
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