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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38718생성일: 2026년 10월 25일

Allyl bromide → 3-Chloro-4-(prop-2-en-1-yloxy)benzaldehyde

https://huagongshe.com/reaction/38718

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물3-Chloro-4-hydroxybenzaldehydeHCID 17022—
반응물Sodium hydrideHCID 24758—
용매WaterHCID 962—
용매tetrahydrofuran N,N-dimethylformamideHCID 21974620—
생성물3-Chloro-4-(prop-2-en-1-yloxy)benzaldehydeHCID 477003685.6%

반응 조건

온도65 °C

반응 단계

To a solution of 3-chloro-4-hydroxybenzaldehyde (5.0 g, 31.9 mmol) in DMF/THF 1:3 (120 mL) is added NaH (1.67 g of a 55% dispersion in mineral oil, 38.3 mmol) in four portions. The mixture is stirred at rt for 1 h before allylbromide (9.66 g, 79.8 mmol) is added. The reaction mixture is heated to 65° C. for 18 h, diluted with water (250 mL) and extracted with diethyl ether (3×250 mL). The organic extracts are washed with water (250 mL), combined and concentrated. The remaining oil is chromatographed on silic gel with heptane/EA 4:1 to afford 4-allyloxy-3-chlorobenzaldehyde (5.37 g) as an almost colourless oil. LC: tR=0.95 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524752B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-482bcd3dcc48433ea236a8b74dc6f9fd
출처 메모uspto-grants-2013_09