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HRID 322932作成日:2026年10月25日

Sodium hydride → methyl (E)-2-benzoylamino-3-(2,4-dibenzyloxyphenyl)acrylate

https://huagongshe.com/reaction/322932

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物2,4-Bis(benzyloxy)benzaldehydeHCID 1809080—
反応物Methyl 2-benzamido-2-(dimethoxyphosphoryl)acetateHCID 14104867—
溶媒TetrahydrofuranHCID 8028—
生成物methyl (E)-2-benzoylamino-3-(2,4-dibenzyloxyphenyl)acrylateHCID 22010495—
生成物methyl (Z)-2-benzoylamino-3-(2,4-dibenzyloxyphenyl)acrylateHCID 70223822—

反応手順

A stirred solution of methyl benzoylamino(dimethoxyphosphoryl)acetate (4.25 g) in dry tetrahydrofuran (30 mL) is treated with sodium hydride (0.66 g, 60% dispersion in mineral oil) under nitrogen. After stirring for 15 minutes a solution of 2,4-dibenzyloxybenzaldehyde (4.74 g) in dry tetrahydrofuran (15 mL) is added dropwise. The reaction mixture is stirred at room temperature for 18 hours, evaporated and the residue partitioned between ethyl acetate (100 mL) and water (75 mL). The organic phase is washed with brine (50 mL), dried over magnesium sulphate and evaporated. The residual yellow oil is purified by flash chromatography on silica eluting with initially with dichloro-methane then with a mixture of dichloromethane and ethyl acetate (9:1 v/v). Fractions homogeneous in the required products are evaporated to give methyl (E)-2-benzoylamino-3-(2,4-dibenzyloxyphenyl)acrylate (1 g) as a yellow foam, and methyl (Z)-2-benzoylamino-3-(2,4-dibenzyloxyphenyl)-acrylate (1.6 g) as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211234B1
出典データセットuspto-grants-2001_04
ORD IDord-da2bc403b35c40529730b4aeab800d13
出典メモuspto-grants-2001_04