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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390694Generated: October 29, 2026

Hydrochloric Acid → (Z)-3-[2-butoxy-3'-(3-heptylureido)biphenyl-4-yl]-2-methoxyacrylic acid

https://huagongshe.com/reaction/390694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
Reactantmethyl (Z)-3-[2-butoxy-3'-(3-heptylureido)biphenyl-4-yl]-2-methoxyacrylateHCID 86626123—
SolventTetrahydrofuranHCID 8028—
Product(Z)-3-[2-butoxy-3'-(3-heptylureido)biphenyl-4-yl]-2-methoxyacrylic acidHCID 1622521785%

Reaction Steps

1.3 mL (1.3 mmol) of aqueous 1 N lithium hydroxide solution are added to a solution of 423 mg (0.87 mmol) of methyl (Z)-3-[2-butoxy-3′-(3-heptylureido)biphenyl-4-yl]-2-methoxyacrylate in 10 mL of tetrahydrofuran. The reaction mixture is stirred for 24 hours at room temperature. After addition of 20 mL of water and acidification with 1 N hydrochloric acid, the reaction medium is extracted with ethyl acetate. The organic phases are combined, washed with saturated sodium chloride solution and dried over sodium sulfate. The solvents are evaporated off and the residue is then recrystallized from 5 mL of acetonitrile. 348 mg (85%) of (Z)-3-[2-butoxy-3′-(3-heptylureido)biphenyl-4-yl]-2-methoxyacrylic acid are obtained in the form of a white powder. (m.p.=137° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-1f51e236e8164d6a97372078a5bd5c83
Source noteuspto-grants-2013_02