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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1527165생성일: 2026년 10월 26일

Acetic Acid → 6-Ethyl-3-formyl-indole-1-carboxylic acid amide

https://huagongshe.com/reaction/1527165

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium hydrideHCID 24758—
반응물Chlorosulfonyl isocyanateHCID 70918—
반응물6-Ethyl-1H-indole-3-carbaldehydeHCID 21850156—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물6-Ethyl-3-formyl-indole-1-carboxylic acid amideHCID 86673790—

반응 조건

온도5 °C

반응 단계

To a solution of NaH (60% in mineral oil, 259 mg, 6.47 mmol) in THF (10 mL) cooled to 5° C. under nitrogen a solution of 6-ethyl-1H-indole-3-carbaldehyde (1.12 g, 6.47 mmol) in THF (20 mL) was slowly added and the mixture was stirred at 5° C. for 30 min. While maintaining the internal temperature between 5° C. and 10° C., chlorosulfonyl isocyanate (1.12 mL, 12.9 mmol) was added dropwise and the solution was further stirred at RT overnight. Acetic acid (15 mL) was added (slightly exothermic) and the solution was stirred at RT for 1.5 h. Ice cubes and water (25 mL) were added, and the solution was further stirred at RT for 30 min. Water was added and the mixture was extracted with EtOAc. The aqueous layer was back-extracted twice with EtOAc. The combined organic layers were dried (Na2SO4), filtered and concentrated. The crude residue was purified by flash column chromatography on silica gel (c-hexane to EtOAc) to give the desired compound. LC/MS: 290.0 [M+H]+, 312.0 [M+Na]+; tR (HPLC conditions a): 3.02 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09085555B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-e9b12aa64ae5409a83b0072d063a41df
출처 메모uspto-grants-2015_07