돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1363282생성일: 2026년 10월 26일

Triphenylphosphine → 4-Benzyl-furan-2-carbaldehyde

https://huagongshe.com/reaction/1363282

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Benzyl diethyl phosphateHCID 298808—
반응물4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-carbaldehydeHCID 3547541—
반응물4-(4-Chlorobenzyl)thiophene-2-carbaldehydeHCID 59648525—
촉매palladium(II) acetateHCID 167845—
용매Acetonitrile 2-propanolHCID 21921005—
생성물4-Benzyl-furan-2-carbaldehydeHCID 5964858541%

반응 단계

The title compound was synthesized from 5-formylfuran-3-boronic acid pinacol ester (878 mg, 3.95 mmol), and benzyl diethyl phosphate (1.25 g, 5.14 mmol) using the same conditions used to synthesize 4-(4-chlorobenzyl)thiophene-2-carbaldehyde, with the exception that triphenylphosphine and Pd(OAc)2 were dissolved in 2:1 CH3CN/isopropyl alcohol. Purification by flash chromatography yielded 4-benzyl-furan-2-carbaldehyde as a white solid (300 mg, 41%). 1H NMR (400 MHz, CDCl3) δ ppm 9.56 (s, 1H) 7.29-7.38 (m, 3H) 7.24-7.28 (m, 2H) 7.17 (d, J=3.5 Hz, 1H) 6.19 (d, J=3.6 Hz, 1H) 4.07 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07884124B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-199dd75aa2af41928e8826721d2e54c7
출처 메모uspto-grants-2011_02