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HRID 475056作成日:2026年10月26日

Benzaldehyde → Ethyl Cinnamate

https://huagongshe.com/reaction/475056

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Triethyl phosphonoacetateHCID 13345—
反応物2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
溶媒DichloromethaneHCID 6344—
生成物Ethyl CinnamateHCID 63775872.4%

反応条件

温度25 °C

反応手順

To a stirred mixture of lithium tert-butoxide (124.6 g, 1.56 mol, 1.10 equiv) in DCM (2000 mL) under N2 at RT was added ethyl 2-(diethoxyphosphoryl)acetate (317 g, 1.41 mol, 1.00 equiv). Benzaldehyde (150 g, 1.41 mol, 1.0 equiv) was then added dropwise to the stirred reaction, and the resulting reaction mixture was stirred under N2 at 25° C. overnight. The reaction mixture was diluted with DCM (2 L). The organic layer was washed with water (3×2 L) and brine (1×2 L), dried (Na2SO4), filtered, and evaporated in vacuo. The crude residue was purified by SiO2 chromatograph eluting with EtOAc/petroleum ether (3.3 to 1% EtOAc) to afford 180 g (72%) of ethyl (2E)-3-phenylprop-2-enoate (31) as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637537B2
出典データセットuspto-grants-2014_01
ORD IDord-2a24aa8a602940fea7000c23a6bea6f5
出典メモuspto-grants-2014_01