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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390611Generated: October 30, 2026

Sodium Hydroxide → 2-[1-[3'-(1-Methyl-3-pentylureido)biphenyl-4-yl]meth-(e)-ylidene]butyric acid

https://huagongshe.com/reaction/390611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-[1-[3'-(1-methyl-3-pentylureido)biphenyl-4-yl]meth-(e)-ylidene]butyrateHCID 68958868—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product2-[1-[3'-(1-Methyl-3-pentylureido)biphenyl-4-yl]meth-(e)-ylidene]butyric acidHCID 1622442484%

Reaction Conditions

Temperature50 °C

Reaction Steps

268 mg (6.7 mmol) of sodium hydroxide are added to a solution of 284 mg (0.67 mmol) of ethyl 2-[1-[3′-(1-methyl-3-pentylureido)biphenyl-4-yl]meth-(E)-ylidene]butyrate in 10 mL of ethanol. The reaction mixture is heated at 50° C. for 15 hours. The reaction medium is evaporated to dryness, taken up in water, acidified with 2 N hydrochloric acid solution and extracted with ethyl acetate. The organic phases are combined, washed with water and dried over magnesium sulfate. After filtration, the solvent is evaporated off and the solid obtained is taken up in ethyl ether, filtered off and dried. 222 mg (84%) of 2-[1-[3′-(1-methyl-3-pentylureido)biphenyl-4-yl]meth-(E)-ylidene]butyric acid are obtained in the form of a white powder with a melting point of 150-152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-b76868267bfa4044a3186fc5f40b8959
Source noteuspto-grants-2013_02