돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10754생성일: 2026년 10월 24일

Benzo(B)Thiophene-2-Boronic Acid → 5-Benzo[b]thiophen-2-yl-2,4-dimethoxy-benzaldehyde

https://huagongshe.com/ko/reaction/10754

반응식

참여 물질

역할이름HCID투입량
반응물Benzo(B)Thiophene-2-Boronic AcidHCID 2359—
반응물Tris(1,1-dimethylethyl)phosphineHCID 83681—
반응물Potassium FluorideHCID 522689—
반응물5-Iodo-2,4-dimethoxybenzaldehydeHCID 14245955—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TetrahydrofuranHCID 8028—
생성물5-Benzo[b]thiophen-2-yl-2,4-dimethoxy-benzaldehydeHCID 16115916—

반응 조건

온도60 °C

반응 단계

Ex-123A: Potassium fluoride (0.42 g, 7.2 mmol), 5-iodo-2,4-dimethoxy-benzaldehyde (Ex-123, 1.0 g, 3.42 mmol), 2-benzo[b]thiophene boronic acid (0.67 g, 3.77 mmol), degased tetrahydrofuran (10 mL), tris(dibenzylideneacetone)dipalladium (19 mg, 0.02 mmol), and tri-tert-butylphosphine (100 mg, 0.05 mmol) were sequentially charged into a flask equipped with a condenser and nitrogen inlet adapter. The reaction mixture was heated at 60° C. for one hour under nitrogen. HPLC analysis indicated of 100% conversion of 5-iodo-2,4-dimethoxy-benzaldehyde (Ex-123) to the title compound prepared through another route (Ex-3A).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094801B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b7422b77623e43858abc2bb907b837a8
출처 메모uspto-grants-2006_08