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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390668Generated: October 30, 2026

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

https://huagongshe.com/reaction/390668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-[1-[2-butoxy-3'-(3-heptyl-1-methylureido)biphenyl-4-yl]meth-(e)-ylidene]butyrateHCID 68959502—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product2-[1-[2-Butoxy-3'-(3-heptyl-1-methylureido)biphenyl-4-yl]meth-(e)-ylidene]butyric acidHCID 1622501076%

Reaction Conditions

Temperature50 °C

Reaction Steps

40 mg (1 mmol) of sodium hydroxide are added to a solution of 531 mg (1 mmol) of ethyl 2-[1-[2-butoxy-3′-(3-heptyl-1-methylureido)biphenyl-4-yl]meth-(E)-ylidene]butyrate in 1 mL of ethanol and 10 mL of tetrahydrofuran. The reaction mixture is heated at 50° C. for 48 hours. The reaction medium is evaporated to dryness, taken up in water, acidified with aqueous 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 oil obtained is purified by chromatography on a column of silica eluted with a 60/40 heptane/ethyl acetate mixture and then precipitated from heptane. 317 mg (76%) of 2-[1-[2-butoxy-3′-(3-heptyl-1-methylureido)biphenyl-4-yl]meth-(E)-ylidene]butyric acid are obtained in the form of a white powder with a melting point of 62-64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-bf618025ad80489eb5ee9b6e6eb6211d
Source noteuspto-grants-2013_02