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HRID 13877作成日:2026年10月25日

Methyl Methacrylate → methyl (2E)-3-[4-(dimethylamino)phenyl]-2-methylprop-2-enoate

https://huagongshe.com/reaction/13877

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl MethacrylateHCID 6658—
反応物4-bromo-N,N-dimethylanilineHCID 11465—
反応物alpha-CyclohexylcyclohexanemethanamineHCID 10774245—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
触媒Tri-tert-butylphosphonium TetraphenylborateHCID 23136663—
溶媒TetrahydrofuranHCID 8028—
生成物methyl (2E)-3-[4-(dimethylamino)phenyl]-2-methylprop-2-enoateHCID 1139036786.7%

反応手順

A 30-ml four-necked flask was equipped with a stirrer, a thermometer and a reflux condenser. 1.000 g (5 mmol) of 4-dimethylaminobromobenzene, 1.001 g (10 mmol) of methyl methacrylate, 0.011 g (0.012 mmol) of tris (dibenzylideneacetone)dipalladium (0), 1.074 g (5.5mmol) of dicyclohexylmethylamine and 5 ml of tetrahydrofuran were weighed in the flask, followed by stirring. Further, 0.026 g (0.05 mmol) of tri-tert-butylphosphonium tetraphenylborate obtained in Example A-1 was weighed in air and added into the flask. The flask was purged with argon, followed by stirring at 30° C. for 25 hours. After the completion of the reaction, 5 ml of toluene and 10 ml of saturated sodium chloride solution were added, followed by separation. The organic phase was purified by column chromatography to afford 0.951 g of (E)-3-(4-dimethylaminophenyl)-2-methylacrylic acid methyl ester (yield: 87 mol % based on 4-dimethylaminobromobenzene). The identification of the product was made by 1H-NMR and 13C-NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728176B2
出典データセットuspto-grants-2010_06
ORD IDord-daee0aff2ff34360b22fd00fcb8d4709
出典メモuspto-grants-2010_06