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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1178944생성일: 2026년 10월 25일

Trifluoroacetic acid → 4-(3-Cyclohexyl-indole-1-sulfonyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/1178944

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물TriethylsilaneHCID 12052—
반응물Sodium BicarbonateHCID 516892—
반응물4-[3-(1-Hydroxy-cyclohexyl)-indole-1-sulfonyl]-benzoic acid methyl esterHCID 58975025—
용매Ethyl AcetateHCID 8857—
생성물4-(3-Cyclohexyl-indole-1-sulfonyl)-benzoic acid methyl esterHCID 5897522087%

반응 단계

Under N2, add triethylsilane (676 mg, 0.929 ml, 5.82 mmol, 2.6 eq) followed by trifluoroacetic acid (4.08 g, 2.7 ml, 35.79 mmol, 16.0 eq) to a CH2CL2 solution (20 ml) of 4-[3-(1-Hydroxy-cyclohexyl)-indole-1-sulfonyl]-benzoic acid methyl ester (925 mg, 2.24 mmol, 1 eq). Stir for 1.5 hours and then remove volatiles on rotovap. Add EtOAc to crude mix and workup with sat aqueous sodium bicarbonate. Extract product into organics, separate organics, dry over MgSO4, and concentrate on rotovap to give crude product as a pink oil. Purify by silica gel chromatography to give 4-(3-Cyclohexyl-indole-1-sulfonyl)-benzoic acid methyl ester (775 mg, 87% yield) as a white solid. Mass Spectrum (m/e): 397.99 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07276516B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-91a319a362c945f89e82beb08f6ffd16
출처 메모uspto-grants-2007_10