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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1826724생성일: 2026년 10월 25일

Water → 5-(2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic acid

https://huagongshe.com/reaction/1826724

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PyridiniumtribromideHCID 21124087—
반응물5-(1H-indol-4-yl)-nicotinic acidHCID 22135477—
촉매ZincHCID 23994—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
용매tert-ButanolHCID 6386—
생성물5-(2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic acidHCID 2213539798%

반응 단계

Pyridinium tribromide (90% (Aldrich), 9.8 g, 27.6 mmol) was added portion-wise over 10 minutes to a suspension of 5-(1H-indol-4-yl)-nicotinic acid (2.2 g, 9.2 mmol) in 2-methyl-2-propanol (54 mL), ethanol (36 mL) and acetic acid (108 mL). The mixture was stirred at room temperature for 2 hours and then acetic acid (10 mL) was added. After stirring for an additional hour, water (0.5 mL) and zinc dust (6 g, 92 mmol) were added and stirring was continued for another hour. Residual zinc dust was filtered and washed with methanol. The filtrate was concentrated and the syrupy residue was stirred in water (300 mL) overnight. The solid which formed was filtered, washed with water to remove zinc and pyridine salts and dried under high vacuum to give 2.3 g (98%) of 5-(2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07053086B2
출처 데이터셋uspto-grants-2006_05
ORD IDord-60aac456ae5e4c0ea4cb52e3e5b69b9c
출처 메모uspto-grants-2006_05