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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390679Generated: October 30, 2026

Water → ethyl (Z)-2-ethoxy-3-[3'-(3-heptyl-1-methylureido)biphenyl-4-yl]acrylate

https://huagongshe.com/reaction/390679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-HeptanamineHCID 8127—
ReactantEthyl AcetateHCID 8857—
Reactantethyl (Z)-2-ethoxy-3-{3'-[methyl(4-nitrophenoxycarbonyl)amino]biphenyl-4-yl}acrylateHCID 86626081—
SolventDimethylformamideHCID 6228—
Productethyl (Z)-2-ethoxy-3-[3'-(3-heptyl-1-methylureido)biphenyl-4-yl]acrylateHCID 8662611677.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

0.31 mL (2.10 mmol) of heptylamine is added to a solution of 0.51 g (1.05 mmol) of ethyl (Z)-2-ethoxy-3-{3′-[methyl-(4-nitrophenoxycarbonyl)amino]biphenyl-4-yl}acrylate in 15 mL of dimethylformamide. The tube is sealed and rapidly placed in an oil bath preheated to 80° C. The reaction mixture is stirred at 80° C. for 1 hour 30 minutes. After cooling, the reaction is worked up by addition of 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 crude product obtained is purified by chromatography on a column of silica eluted with a 75/25 heptane/ethyl acetate mixture to give 0.38 g (77%) of ethyl (Z)-2-ethoxy-3-[3′-(3-heptyl-1-methylureido)biphenyl-4-yl]acrylate in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-2f705ae33aaf46a6b8071434bb0fe465
Source noteuspto-grants-2013_02