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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1017002생성일: 2026년 10월 24일

Toluene → 3-(Furan-3-yl)benzaldehyde

https://huagongshe.com/ko/reaction/1017002

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Potassium CarbonateHCID 11430—
반응물3-BromofuranHCID 89164—
반응물3-Formylphenylboronic acidHCID 2734356—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-(Furan-3-yl)benzaldehydeHCID 2350601010%

반응 단계

EX-601A) To a toluene (10 mL) solution of 3-bromofuran (0.54 mL, 6.0 mmol) was added 3-formylphenylboronic acid (1.00 g, 6.7 mmol) and DMF (4 mL). To the resulting solution was added K2CO3 (1.85 g, 13.4 mmol) and Pd(PPh3)4 (0.40 g, 0.35 mmol). The slurry was heated to reflux under argon for 2 h. The cooled mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4) and evaporated to an oil. Purification by flash chromatography on silica gel eluting with 5% ethyl acetate in hexane gave 0.10 g (10%) of the desired 3-(3-furanyl)benzaldehyde product as a yellow oil. MS: m/z=173.0 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06476057B1
출처 데이터셋uspto-grants-2002_11
ORD IDord-0e96dedeb2db434abd0ebaa704af1346
출처 메모uspto-grants-2002_11