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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2108876생성일: 2026년 10월 26일

Chloroform → 4-[(5-Bromopentyl)sulfanyl]-7-(trifluoromethyl)quinoline

https://huagongshe.com/reaction/2108876

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물1,5-DibromopentaneHCID 8100—
반응물Potassium CarbonateHCID 11430—
반응물HCID 178506078HCID 178506078—
촉매Tetrabutylammonium BromideHCID 74236—
용매WaterHCID 962—
생성물4-[(5-Bromopentyl)sulfanyl]-7-(trifluoromethyl)quinolineHCID 1797581572%

반응 조건

온도20 °C

반응 단계

7-Trifluoromethyl-4-quinoline-thiol (5 g, 21.8 mmol), 1,5-dibromopentane (23.7 g, 98.1 mmol) and CHCl3 (60 mL) were charged in a 250 ml round-bottomed flask equipped with a magnetic stirrer. TBABr (0.7 g, 2.2 mmol) and water (40 mL) were added and the reaction mixture was stirred for 48 h at 20° C. The reaction mixture was poured in 100 mL of H2O with K2CO3 (3.0 g, 21.8 mmol) and extracted with CH2Cl2 (400 mL). The organic layer was washed with water (30 mL), brine (2×30 mL), dried over MgSO4, filtered and evaporated at 30° C. to dryness. The crude compound was purified by column chromatography (SiO2:CH2Cl2:MeOH=99.5:0.5 to 98:2) to give after evaporation 4-(5-bromopentylthio)-7-(trifluoromethyl)quinoline 25 (5.9 g, 72% yield) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07514432B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-5ddb69884b0e43a7837a8afe289ae646
출처 메모uspto-grants-2009_04