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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250863Generated: October 26, 2026

Acetic Acid → 3-[3'-(3-Heptyl-1-methylureido)-2-methylbiphenyl-4-yl]propanoic acid

https://huagongshe.com/reaction/250863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantMeOH tetrahydrofuranHCID 21899815—
ReactantEthyl 3-{3'-[1-methyl-3-(3-phenylpropyl)ureido]biphenyl-4-yl}propanoateHCID 67272529—
Product3-[3'-(3-Heptyl-1-methylureido)-2-methylbiphenyl-4-yl]propanoic acidHCID 1171851955%

Reaction Steps

100 mg (2.5 mmol, 3.2 eq) of sodium hydroxide are added to a solution of 348 mg (0.78 mmol, 1 eq) of ethyl 3-{3′-[1-methyl-3-(3-phenylpropyl)ureido]biphenyl-4-yl}propanoate in 6 ml of a tetrahydrofuran/methanol mixture (8/2). The reaction mixture is stirred at room temperature for 12 hours. The reaction medium is hydrolyzed with water, acidified with acetic acid solution and extracted with ethyl acetate. The organic phases are combined, washed with sodium chloride solution and dried over sodium sulfate. The solvent is evaporated off and the residual oil is chromatographed on silica (7/3 to 1/1 heptane/ethyl acetate). 180 mg of 3-[3′-(3-heptyl-1-methylureido)-2-methylbiphenyl-4-yl]propanoic acid are obtained in the form of a tacky solid. Yield=55%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863332B2
Source datasetuspto-grants-2011_01
ORD IDord-6f40237e50844070b072f73b0b73b058
Source noteuspto-grants-2011_01