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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 351588생성일: 2026년 10월 26일

Indole-7-carboxaldehyde → 7-Ethenyl-1H-indole

https://huagongshe.com/reaction/351588

반응식

참여 물질

역할이름HCID투입량
반응물Indole-7-carboxaldehydeHCID 2734629—
반응물Potassium tert-butoxideHCID 23665647—
촉매Methyltriphenyliphosphonium bromideHCID 74505—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물7-Ethenyl-1H-indoleHCID 14567404—

반응 단계

To a solution of methyl triphenylphosphonium bromide (5.05 g, 14.1 mmol) in tetrahydrofuran (80 mL) was added potassium tert-butoxide (1 M in tetrahydrofuran, 14.1 mL, 14.1 mmol) and the reaction stirred for 45 minutes at room temperature. Next a prepared solution of 7-formylindole (1.00 g, 6.89 mmol) in tetrahydrofuran (10 mL) was added and the reaction stirred for 1.5 hours. The reaction mixture was diluted with ethyl acetate (250 mL) and washed with an 8:1 mixture of water and 1 N hydrochloric acid (2×100 mL), saturated aqueous sodium chloride (100 mL), and dried over sodium sulfate. The solution was filtered and the filtrate concentrated under reduced pressure. The residue was subjected to silica gel chromatography. Fractions containing product were combined and concentrated under reduced pressure to provide the desired compound as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743785B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-43a1ca3d2ecd4c47834d89a23cb06795
출처 메모uspto-grants-2004_06