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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642117Generated: October 27, 2026

3-(3'-Hydroxyphenyl)propionic acid → Methyl 4-{[3-(3-hydroxyphenyl)propanoyl]amino}benzoate

https://huagongshe.com/reaction/642117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(3'-Hydroxyphenyl)propionic acidHCID 91—
Reactant4-MethylmorpholineHCID 7972—
ReactantMethyl 4-aminobenzoateHCID 12082—
ReactantIsobutyl chloroformateHCID 62365—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-{[3-(3-hydroxyphenyl)propanoyl]amino}benzoateHCID 6840925132%

Reaction Steps

To a solution of 3-(3-hydroxyphenyl)-propionic acid (198 mg, 1.19 mmol) in anhydrous THF (5 mL) were added N-methylmorpholine (1.2 equiv.) and isobutylchloroformate (1.2 equiv.) at 0° C. After 30 min, at 0° C., a solution of methyl 4-aminobenzoate (150 mg, 0.99 mmol) in anhydrous THF (1 mL) was added to the reaction mixture. After 5 min the temperature was allowed to warm up to rt and stir overnight. After extraction with EtOAc (100 mL), washing with HCl (0.1N, 50 mL) and a saturated aqueous solution of NaHCO3 (50 mL), the organic layer was dryed over sodium sulfate and evaporated under vacuo to give a yellow oil. Purification by flash chromatography using EtOAc/cyclohexane as eluant and recrystallization from DCM/MeOH/TEA (10/0.4/0.1) gave the title compound as a white solid (32%) in 98.9% purity by HPLC (MaxPlot detection between 230 and 400 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696231B2
Source datasetuspto-grants-2010_04
ORD IDord-e29aac5a86d041d58b68ec7d2515d364
Source noteuspto-grants-2010_04