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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1363249생성일: 2026년 10월 27일

Triphenylphosphine → 4-(4-Chlorobenzyl)thiophene-2-carbaldehyde

https://huagongshe.com/reaction/1363249

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물2-Formylthiophene-4-boronic acidHCID 11084115—
반응물4-Chlorobenzyl diethyl phosphateHCID 11277438—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
생성물4-(4-Chlorobenzyl)thiophene-2-carbaldehydeHCID 5964852528%

반응 조건

온도90 °C

반응 단계

A solution mixture of Pd(OAc)2 (144 mg, 0.64 mmol) and triphenylphosphine (TPP) (136 mg, 0.52 mmol) were weighed into a vial, dissolved in acetonitrile and transferred into a 40 mL Wheaton vial containing diethyl 4-chlorobenzyl phosphate (Org. Lett. 2005, 7, 4875-4878; 3.08 g, 11.6 mmol), 5-formylthiophen-3-ylboronic acid (2.0 g, 12.8 mmol), K3PO4 (2.72 g, 12.8 mmol) and a stir-bar. Nitrogen gas was bubbled through the mixture. The vial was closed tightly and heated to 90° C. and vigorously stirred for 16 h. The reaction was diluted with water and extracted with dichloromethane (DCM) (3×100 mL). The combined extracts were washed with brine, dried over Na2SO4, filtered and concentrated. Purification by flash chromatography (Isco CombiFlash) (0-20% heptane/EtOAc) yielded 4-(4-chlorobenzyl)thiophene-2-carbaldehyde: 835 mg, 28% yield. 1H NMR (400 MHz, CDCl3) δ ppm: 10.10 (d, 1H), 7.80 (d, 1H), 7.63 (m, 1H), 7.55 (m, 2H), 7.40 (m, 2H), 4.23 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07884124B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-b2a23646235e488e853b624b000ddd59
출처 메모uspto-grants-2011_02