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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Hydroxyphenyl)propionic acidHCID 10394—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-EthoxyphenethylamineHCID 142362—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-[2-(2-ethoxyphenyl)ethyl]-3-(4-hydroxyphenyl)propanamideHCID 68873053104.2%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521461B2
Source datasetuspto-grants-2009_04
ORD IDord-af8ff9fcbf7b4f3da9f3456e11896101
Source noteuspto-grants-2009_04