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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508022Generated: November 2, 2026

Citric Acid → 3-{4-[[(2',6'-Dimethylbiphenyl-3-yl)methyl](propyl)amino]phenyl}propanoic acid

https://huagongshe.com/reaction/508022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-{4-[[(2',6'-dimethylbiphenyl-3-yl)methyl](propyl)amino]phenyl}propanoateHCID 23157276—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-{4-[[(2',6'-Dimethylbiphenyl-3-yl)methyl](propyl)amino]phenyl}propanoic acidHCID 2315725299.9%

Reaction Steps

To a solution of methyl 3-{4-[[(2′,6′-dimethylbiphenyl-3-yl)methyl](propyl)amino]phenyl}propanoate (0.735 g, 1.77 mmol) in a mixture of methanol (8 mL) and tetrahydrofuran (8 mL) was added 2 M aqueous sodium hydroxide solution (2.5 mL), and the mixture was stirred at room temperature for 19 hr. Water was added to the reaction mixture, and the mixture was weakly acidified with 10% aqueous citric acid solution and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (20%-70% ethyl acetate/hexane) to give the title compound (0.710 g, yield 99%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-86ae48b9775544089406e92e1cdb102e
Source noteuspto-grants-2010_08