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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428710생성일: 2026년 10월 26일

Triethylamine → 4-[(E)-2-(2-chlorophenyl)-ethenyl]-1,3-dihydro-(Z)-3-[(1H-pyrrol-2-yl)methylene]-2H-indol-2-one

https://huagongshe.com/reaction/428710

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-ChlorostyreneHCID 14906—
반응물Tri-o-tolylphosphineHCID 80271—
반응물(Z)-1,3-dihydro-4-iodo-3-[(1H-pyrrol-2-yl)methylene]-indol-2-oneHCID 15548052—
용매DimethylformamideHCID 6228—
생성물4-[(E)-2-(2-chlorophenyl)-ethenyl]-1,3-dihydro-(Z)-3-[(1H-pyrrol-2-yl)methylene]-2H-indol-2-oneHCID 9906247—

반응 단계

A solution of (Z)-1,3-dihydro-4-iodo-3-[(1H-pyrrol-2-yl)methylene]-2H-indol-2-one (39 mg, 0.116 mmol) (from Example 71 above), triethylamine (65 μL, 0.464 mmol), tri-o-tolylphosphine (7 mg, 0.023 mmol) (Aldrich), palladium(ll) acetate (2 mg, 0.009 mmol) (Aldrich), and 2-chlorostyrene (24 mg, 0.173 mmol) (Aldrich) in 3 mL of dry N,N-dimethylformamide was heated at 85° C. under a nitrogen atmosphere for 20 h. The reaction mixture was allowed to cool to room temperature and then directly purified by flash chromatography (Merck Silica gel 60, 230-400 mesh, 5% ethyl acetate-benzene elution) to yield pure 4-[(E)-2-(2-chlorophenyl)-ethenyl]-1,3-dihydro-(Z)-3-[(1H-pyrrol-2-yl)methylene]-2H-indol-2-one as a yellow solid. (Yield 27 mg, 67%; mp=257-258° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313310B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-d6fc4078a5ef46a887808e870e3912bc
출처 메모uspto-grants-2001_11