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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390617Generated: October 29, 2026

Acetic Acid → HCID 16226559, compound

https://huagongshe.com/reaction/390617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 16224425HCID 16224425—
SolventTetrahydrofuranHCID 8028—
ProductHCID 16226559HCID 1622655977%

Reaction Conditions

Temperature68 °C

Reaction Steps

2.7 mL (2.7 mmol) of aqueous 1 N sodium hydroxide solution are added to a solution of 0.7 g (1.8 mmol) of methyl (Z)-3-[3′-(3-butyl-1-methylureido)biphenyl-4-yl]-2-methoxyacrylate in 12 mL of tetrahydrofuran. The reaction medium is heated at 68° C. and stirred for 2 hours. The reaction medium is acidified with 2.8 mL of 1 N acetic acid solution and extracted with ethyl acetate. The organic phase is washed with water, dried over magnesium sulfate, filtered and evaporated. The residue obtained is recrystallized from hot ethyl acetate. 530 mg (77%) of (Z)-3-[3′-(3-butyl-1-methylureido)biphenyl-4-yl]-2-methoxyacrylic acid are obtained in the form of a white solid with a melting point of 146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-2b08c7095c52424c8857a8f1cb733973
Source noteuspto-grants-2013_02