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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2264630생성일: 2026년 10월 25일

Sodium Chloride → ethyl (2Z)-3-{1-[(4-bromophenyl)sulfonyl]-1H-indol-2-yl}acrylate

https://huagongshe.com/reaction/2264630

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Ethyl Di-o-tolylphosphonoacetateHCID 10593815—
반응물Benzyltrimethylammonium hydroxide methanolHCID 19865511—
반응물1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carbaldehydeHCID 44210807—
용매TetrahydrofuranHCID 8028—
생성물ethyl (2Z)-3-{1-[(4-bromophenyl)sulfonyl]-1H-indol-2-yl}acrylateHCID 67044639—

반응 조건

온도-70 °C

반응 단계

To a solution of 0.4 mL of ethyl di-o-tolylphosphonoacetate in 15 mL of THF was added 0.67 g of a 40% benzyltrimethylammonium hydroxide-methanol solution under cooling in a dry ice-acetone bath, and the resulting mixture was stirred at −70° C. for 15 minutes. To the solution, a solution of 0.47 g of 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carbaldehyde in 5 mL of THF was added, the resulting mixture was stirred at −70° C. for 1.5 hours and under cooling in an ice-methanol bath for 1 hour. To the solution, 50 mL of saturated aqueous sodium chloride solution was added, the mixture was extracted with 100 mL of ethyl acetate, the extract was washed with water and saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-hexane=1:5) to obtain 0.53 g of ethyl (2Z)-3-{1-[(4-bromophenyl)sulfonyl]-1H-indol-2-yl}acrylate as a pale yellow syrup. ESI−: 432, 434

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07855225B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-97cd595b10774946a0ddfbc9411f72dc
출처 메모uspto-grants-2010_12