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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390639Generated: October 28, 2026

Hydrochloric Acid → HCID 16224621, compound

https://huagongshe.com/reaction/390639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86626094HCID 86626094—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 16224621HCID 1622462177.1%

Reaction Conditions

Temperature68 °C

Reaction Steps

1.24 mL (1.24 mmol) of aqueous 1 M sodium hydroxide solution are added to a solution of 0.4 g (0.83 mmol) of methyl (Z)-3-[2-butoxy-3′-(1-methyl-3-pentylureido)biphenyl-4-yl]-2-methoxyacrylate in 10 mL of tetrahydrofuran. The reaction mixture is stirred at 68° C. for 5 hours. After cooling, the reaction is worked up by addition of 3 mL (3 mmol) of aqueous 1 M hydrochloric acid solution and 10 mL of water and extraction with ethyl acetate. The organic phases are combined, washed with saturated sodium chloride solution and then dried over magnesium sulfate. The solvents are evaporated off. The product is recrystallized from a pentane/acetone mixture to give 0.3 g (76%) of (Z)-3-[2-butoxy-3′-(1-methyl-3-pentylureido)biphenyl-4-yl]-2-methoxyacrylic acid in the form of a cream-colored solid with a melting point of 61° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-c53fdd44bfd442e688aafcb7781da4e5
Source noteuspto-grants-2013_02