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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1099057생성일: 2026년 10월 25일

1-Bromo-2-Chloroethane → 1-(Quinolin-6-yl)cyclopropanecarbonitrile

https://huagongshe.com/reaction/1099057

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-2-ChloroethaneHCID 7849—
반응물Sodium HydroxideHCID 14798—
반응물(Quinolin-6-yl)acetonitrileHCID 21992552—
촉매Benzyl triethylammonium chlorideHCID 66133—
용매WaterHCID 962—
생성물1-(Quinolin-6-yl)cyclopropanecarbonitrileHCID 6681284096%

반응 조건

온도50 °C

반응 단계

60 mL of 50% aqueous NaOH was added to a mixture of 1-bromo-2-chloroethane (22.0 mL, 0.265 mol), quinolin-6-ylacetonitrile (16.0 g, 0.0666 mol), and benzyltriethylammonium chloride (0.99 g, 0.0043 mol) at 50° C. The mixture was stirred at 50° C. for 3 h. After cooling to RT, the reaction mixture was poured into 100 ml of water, and extracted with DCM (3×100 mL). The combined organic layers were dried over anhydrous Na2SO4, filtered through a pad of silica gel and washed with ethyl acetate in DCM (20%). The filtrate was concentrated to give the crude product 1-quinolin-6-ylcyclopropanecarbonitrile (12.4 g, 96%) which was directly used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143251B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-0a3565002521440ca8d750e627d3c973
출처 메모uspto-grants-2012_03