돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74465생성일: 2026년 10월 24일

Ethyl Propionate → 5-bromo-1-(toluene-4-sulfonyl)-6-trifluoromethyl-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/74465

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl PropionateHCID 7749—
반응물DiisopropylethylamineHCID 81531—
반응물N-(4-bromo-2-iodo-5-trifluoromethyl-phenyl)-4-methyl-benzenesulfonamideHCID 68005027—
촉매Zinc bromideHCID 10421208—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물5-bromo-1-(toluene-4-sulfonyl)-6-trifluoromethyl-1H-indole-2-carboxylic acid ethyl esterHCID 68004700—

반응 조건

온도80 °C

반응 단계

N,N-diisopropylethyl amine (0.42 ml, 2.4 mmol), ethyl propionate (0.12 ml, 1.2 mmol), and tetrakis(triphenylphosphine)palladium (46 mg, 0.04 mmol) were added to an anhydrous tetrahydrofuran (THF) solution (3.2 ml) containing N-(4-bromo-2-iodo-5-trifluoromethyl-phenyl)-4-methyl-benzenesulfonamide (208 mg, 0.4 mmol) and zinc bromide (270 mg, 1.2 mmol). Then, the mixture was evacuated, and backfilled with argon. This was stirred at 80° C. for 13 hours. After cooling it to room temperature, the reaction mixture was filtered through Celite, and washed with ethyl acetate. The wash solution was washed with an aqueous solution saturated with sodium bicarbonate and an aqueous solution saturated with sodium chloride, and dried over anhydrous sodium sulfate. The desiccant was removed by filtration, and concentration was performed. Then, the residue obtained by concentration under reduced pressure was purified by silica gel column chromatography. Thus, 5-bromo-1-(toluene-4-sulfonyl)-6-trifluoromethyl-1H-indole-2-carboxylic acid ethyl ester was obtained as a pale brown solid (195 mg, 50%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829199B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-bd000ac9664b45088171998e60399da1
출처 메모uspto-grants-2014_09