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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390650Generated: October 25, 2026

Water → ethyl (E)-2-methyl-3-(3'-methylaminobiphenyl-4-yl)acrylate

https://huagongshe.com/reaction/390650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant[3-(Methylamino)phenyl]boronic acidHCID 23558980—
Reactantethyl (E)-3-(4-iodo-3-propoxyphenyl)-2-methylacrylateHCID 86626099—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
SolventPotassium Phosphate, TribasicHCID 62657—
Productethyl (E)-2-methyl-3-(3'-methylaminobiphenyl-4-yl)acrylateHCID 6895715378.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

1.6 g (4.3 mmol) of ethyl (E)-3-(4-iodo-3-propoxyphenyl)-2-methylacrylate are dissolved in 10 mL of a 4/1v/v mixture of dimethylformamide and of aqueous 2 M potassium phosphate solution. 0.9 g (5.7 mmol) of 3-methylaminophenylboronic acid prepared as described in Example 31e, 58 mg (0.2 mmol) of palladium acetate and 152 mg (0.4 mmol) of dicyclohexylbiphenylphosphine are added. The mixture is stirred for 3 hours at 90° C. After cooling and adding water, the medium is extracted with ethyl acetate. The organic phase is washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with an 8/2 heptane/ethyl acetate mixture. 1.0 g (65%) of ethyl (E)-2-methyl-3-(3′-methylaminobiphenyl-4-yl)acrylate is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-e1edcaf21acc4dd19f211f0a5f40af81
Source noteuspto-grants-2013_02