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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 855280생성일: 2026년 10월 23일

Carbon Dioxide → 5-methyl-1H-indole-7-carboxylic acid

https://huagongshe.com/ko/reaction/855280

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물WaterHCID 962—
반응물7-Bromo-5-methyl-1H-indoleHCID 3403330—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물5-methyl-1H-indole-7-carboxylic acidHCID 6686836156%

반응 조건

온도2.5 °C

반응 단계

1.68 g of 7-bromo-5-methyl-indole (8 mmol) were dissolved in 30 ml THF and 15 ml of a 1.6 molar solution of n-BuLi in hexane were added at −78° C. The reaction mixture was then allowed to warm to 0-5° C. and was stirred at this temperature for 30 min. Then it was cooled again to −78° C., dry ice was added and the mixture was allowed to warm to rt. After 15 min at rt it was poured into water and extracted twice with ether. The aqueous phase was then acidified with 1 N HCl solution and extracted several times with DCM. The combined DCM extracts were then washed with brine, dried with magnesium sulfate, filtered and the solvent was evaporated. The remaining residue was triturated with n-hexane. Final filtration yielded 0.78 g (56%) of 5-methyl-1H-indole-7-carboxylic acid as light brown solid. 1H NMR (DMSO-d, 300 MHz): δ 2.41 (s, 3H), 6.44 (m, 1H), 7.31 (m, 1H), 7.58 (s, 1H), 7.61 (s, 1H), 10.91 (br s, 1H), 12.92 (br s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259183B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-5721f061e67e4ef3ada7bb121c21c9a0
출처 메모uspto-grants-2007_08