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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428705생성일: 2026년 10월 24일

Benzaldehyde → rac-(Z)-1,3-dihydro-4-(3-hydroxy-3-phenyl-1-propynyl)-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-one

https://huagongshe.com/ko/reaction/428705

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물alpha-EthynylbenzenemethanolHCID 20155—
반응물(Z)-4-bromo-1,3-dihydro-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-oneHCID 18359254—
반응물HCID 178462451HCID 178462451—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물rac-(Z)-1,3-dihydro-4-(3-hydroxy-3-phenyl-1-propynyl)-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-oneHCID 9969383—

반응 단계

Using Method D above, 3-hydroxy-3-phenyl-1-propyne (0.1 g, 0.78 mmol) (prepared by the addition of ethynylmagnesium chloride (Aldrich) to benzaldehyde (Aldrich) through Method A above) was coupled to (Z)-4-bromo-1,3-dihydro-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-one (0.1 g, 0.31 mmol) (Starting Material 1) using DPPFPdCl2 (12.6 mg) (Aldrich) and CuI (3 mg) (Aldrich) as catalyst in DMF (5 mL) and Et3N (5 mL) as solvent at 85° C. for 18 h, yielding rac-(Z)-1,3-dihydro-4-(3-hydroxy-3-phenyl-1-propynyl)-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-one. (Yield 42 mg, 38%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313310B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-023af678f9a34135891f01370728af4e
출처 메모uspto-grants-2001_11