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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390654Generated: October 31, 2026

Ammonium Chloride → ethyl (E)-3-(2-ethoxy-3' methylaminobiphenyl-4-yl)-2-methylacrylate

https://huagongshe.com/reaction/390654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-(Dicyclohexylphosphino)biphenylHCID 2734216—
ReactantN-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 57976762—
Reactantethyl (E)-3-(3-ethoxy-4-trifluoromethanesulfonyloxyphenyl)-2-methylacrylateHCID 86626100—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Productethyl (E)-3-(2-ethoxy-3' methylaminobiphenyl-4-yl)-2-methylacrylateHCID 8662610225.5%

Reaction Conditions

Temperature92.5 °C

Reaction Steps

45 mg (0.2 mmol) of palladium acetate and then 140 mg (0.4 mmol) of 2-(dicyclohexylphosphino)biphenyl are added to a mixture of 1.65 g (4 mmol) of ethyl (E)-3-(3-ethoxy-4-trifluoromethanesulfonyloxyphenyl)-2-methylacrylate, 1.1 g (4.8 mmol) of methyl[3-(4,4,5,5-tetramethyl[1.3.2]dioxaborolan-2-yl)phenyl]amine (prepared as described in Example 28a) and 2 mL of aqueous 2 M potassium phosphate solution in 8 mL of dimethylformamide. The reaction mixture is heated at 90-95° C. for 4 hours. The medium is hydrolyzed with saturated ammonium chloride solution and extracted with ethyl acetate. The organic phases are combined, washed with saturated sodium chloride solution and dried over sodium sulfate. The solvent is evaporated off and the brown oil obtained (2.7 g) is purified by chromatography on a column of silica eluted with a 90/10 heptane/ethyl acetate mixture. 346 mg (17%) of ethyl (E)-3-(2-ethoxy-3′ methylaminobiphenyl-4-yl)-2-methylacrylate 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-1ecd4859918647fa9eda5321f2b14a48
Source noteuspto-grants-2013_02