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HRID 131771作成日:2026年10月27日

Hydrochloric Acid → (E)-N,N-diisopropyl-3-(2-methoxy-5-methoxycarbonylphenyl)acrylamide

https://huagongshe.com/reaction/131771

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物N,N-DimethylglycineHCID 673—
反応物Sodium AcetateHCID 517045—
反応物N,N-DiisopropylacrylamideHCID 559397—
反応物Methyl 3-bromo-4-methoxybenzoateHCID 611662—
溶媒DichloromethaneHCID 6344—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物(E)-N,N-diisopropyl-3-(2-methoxy-5-methoxycarbonylphenyl)acrylamideHCID 2273520969%

反応条件

温度130 °C

反応手順

A stirred suspension consisting of N,N-dimethylglycine (6.0 mmol), anhydrous sodium acetate (40 mmol), methyl 3-bromo-4-methoxybenzoate (20 mmol, 4.90 g), N,N-diisopropylacrylamide (24 mmol, 3.72 g), bis-(benzonitrile)-palladium-II chloride (1.5 mol %), and 20 ml of N-methyl-2-pyrrolidinone was heated at 130° C. until no starting material could be detected by tlc (starting material methyl 3-bromo-4-methoxybenzoate: Rf 0.73; N,N-diisopropylacrylamide: Rf 0.46; solvent system (1)). After cooling to room temperature 50 ml of an aqueous 2N HCl solution was added. The reaction was diluted with dichloromethane (50 ml) and the precipitated grey palladium metal was filtered off. The organic phase was washed with five portions (50 ml each) of 2N aqueous hydrochloric acid, dried (MgSO4) and evaporated to dryness. The remaining off-white solid was recrystallized from ethyl acetate/n-hexane to give 4.40 g (E)-N,N-diisopropyl-3-(2-methoxy-5-methoxycarbonylphenyl)acrylamide in 69% yield, m.p. 139-140° C., tlc: (1) Rf 0.40. NMR (CD2Cl2): 21.22, 22.10, 46.39, 48.87, 52.59, 56.61, 111.42, 123.39, 123.78, 125.54, 130.32, 132.53, 135.07. MS (EI, DI, 105° C.): 319 (M+−, 22), 304 (6%), 276 (8%), 219 (100%), 187 (18%), 160 (7%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384980B2
出典データセットuspto-grants-2008_06
ORD IDord-93fe49f43b884d8ca5e3a57f0dbc6d33
出典メモuspto-grants-2008_06