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HRID 468878作成日:2026年10月25日

2-Chlorobenzaldehyde → 1-Chloro-2-(2-methoxyvinyl)benzene

https://huagongshe.com/reaction/468878

反応式

関与物質

役割名称HCID仕込み量
反応物2-ChlorobenzaldehydeHCID 6996—
反応物Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物1-Chloro-2-(2-methoxyvinyl)benzeneHCID 54178283101.7%

反応手順

To a stirred solution of (methoxymethyl)triphenylphosphonium chloride (10 g, 28 mmol) in tetrahydrofuran (46 mL) cooled at −15° C. was added potassium tert-butoxide (3.7 g, 31 mmol) as a solid in one portion. After 5 minutes, 2-chlorobenzaldehyde (2.0 g, 14 mmol) was added, and the reaction mixture was warmed to room temperature and stirred for two hours. The reaction was quenched with saturated aqueous ammonium chloride solution (5 mL), tetrahydrofuran evaporated in vacuo, and the resulting residue was diluted with diethyl ether (100 mL) and water (100 mL). The organic layer was separated, dried over sodium sulfate, filtered, and evaporated in vacuo to afford a residue that was purified by flash chromatography (silica, 80 g, ISCO, 0-10% ethyl acetate in heptane) to afford the title compound as a colorless oil (2.4 g, 100%), which was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08623889B2
出典データセットuspto-grants-2014_01
ORD IDord-a2d6b2c123b644ffbea7cebcdd252996
出典メモuspto-grants-2014_01