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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24488생성일: 2026년 10월 24일

Indole-2-carboxaldehyde → 3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acid

https://huagongshe.com/ko/reaction/24488

반응식

참여 물질

역할이름HCID투입량
반응물Indole-2-carboxaldehydeHCID 96389—
반응물2-Oxindole-5-carboxylic acidHCID 2773318—
촉매PiperidineHCID 8082—
용매EthanolHCID 702—
생성물3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acidHCID 5409037040%

반응 단계

A mixture of 5-carboxy-2-oxindole (88.5 mg), indole-2-carbaldehyde (87 mg) (prepared according to Synthetic Communications, 1993, 23, 3109) and piperidine (1 drop) in ethanol (3 mL) was held in a sealed tube at 95° C. for 4 hours. The mixture was cooled to room temperature. The solid was filtered and acidified with 2N hydrochloric acid. The resulting solid was collected by vacuum filtration, washed with cold ethanol and dried in vacuum oven to give 60 mg (40% yield) of 3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-carboxylic acid as a mustard-colored solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-357e9239ad554dfba41aa9ad2f1e3a97
출처 메모uspto-grants-2005_02