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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390612Generated: October 29, 2026

Sodium Carbonate → ethyl (Z)-2-ethoxy-3-(3'-methylaminobiphenyl-4-yl)acrylate

https://huagongshe.com/reaction/390612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantN-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 57976762—
Reactantethyl (Z)-3-(4-bromophenyl)-2-ethoxyacrylateHCID 68960230—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Productethyl (Z)-2-ethoxy-3-(3'-methylaminobiphenyl-4-yl)acrylateHCID 8662607994%

Reaction Steps

To a solution of 10.8 g (36.1 mmol) of ethyl (Z)-3-(4-bromophenyl)-2-ethoxyacrylate, 108 mL (217 mmol) in 120 mL of toluene, aqueous 2 M sodium carbonate solution and 1.5 g (1.8 mmol) of dichloro[11′-bis(diphenylphosphino)ferrocene]palladium are added. The reaction medium is stirred and 9.25 g (39.7 mmol) of methyl[3-(4,4,5,5-tetramethyl[1.3.2]dioxaborolan-2-yl)phenyl]amine are then added. After stirring at 80° C. for 2 hours, the reaction medium is hydrolyzed and diluted with ethyl acetate. After separation of the phases by settling, the ethyl acetate phase is washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with a 90/10 and then 80/20 heptane/ethyl acetate mixture. 10.5 g (94%) of ethyl (Z)-2-ethoxy-3-(3′-methylaminobiphenyl-4-yl)acrylate are obtained in the form of a yellow oil. After taking up the product in pentane, 9.5 g (85%) of ethyl (Z)-2-ethoxy-3-(3′-methylaminobiphenyl-4-yl)acrylate are obtained in the form of a pale yellow solid with a melting point of 52° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-17f9cc55510a431aa6427139e6a61fd6
Source noteuspto-grants-2013_02