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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1502395생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1502395

반응식

참여 물질

역할이름HCID투입량
반응물2-ChlorobenzaldehydeHCID 6996—
반응물Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물1-Chloro-2-(2-methoxyvinyl)benzeneHCID 54178283101.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09206175B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-46ad1198f94e46db99a9b9903368fe9a
출처 메모uspto-grants-2015_12