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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390678Generated: November 1, 2026

Water → ethyl (Z)-2-ethoxy-3-{3'-[methyl(4-nitrophenoxycarbonyl)amino]biphenyl-4-yl}acrylate

https://huagongshe.com/reaction/390678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethylamineHCID 8021—
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactantethyl (Z)-2-ethoxy-3-(3'-methylaminobiphenyl-4-yl)acrylateHCID 86626079—
SolventDichloromethaneHCID 6344—
Productethyl (Z)-2-ethoxy-3-{3'-[methyl(4-nitrophenoxycarbonyl)amino]biphenyl-4-yl}acrylateHCID 86626081126.2%

Reaction Steps

0.63 g (3.1 mmol) of 4-nitrophenyl chloroformate and then 0.54 mL (3.1 mmol) of diethylamine are added to a solution of 0.68 g (2.1 mmol) of ethyl (Z)-2-ethoxy-3-(3′-methylaminobiphenyl-4-yl)acrylate in 15 mL of dichloromethane. The reaction mixture is stirred for 1 hour 30 minutes at room temperature. The reaction is worked up by addition of 10 mL of water and then extracted with dichloromethane. The organic phases are combined and then dried over magnesium sulfate. The solvents are evaporated off. 1.3 g (100%) of ethyl (Z)-2-ethoxy-3-{3′-[methyl-(4-nitrophenoxycarbonyl)amino]biphenyl-4-yl}acrylate are obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-fa17fca0c2414bec984c3b6134d3eb22
Source noteuspto-grants-2013_02