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HRID 13896作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/13896

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 tetra-para-tolylborateHCID 23136639—
溶媒TetrahydrofuranHCID 8028—
生成物methyl (2E)-3-[4-(dimethylamino)phenyl]-2-methylprop-2-enoateHCID 1139036787%

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 (5.5 mmol) of dicyclohexylmethylamine and 5 ml of tetrahydrofuran were weighed in the flask, followed by stirring. Further, 0.029 g (0.05 mmol) of tri-tert-butylphosphonium tetra-para-tolylborate obtained in Example B-3 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 0.954 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 H-NMR and 3C-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-b0ed96f2a095420cbe1c0169339b4132
出典メモuspto-grants-2010_06