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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 333752생성일: 2026년 10월 24일

Azobisisobutyronitrile → 7-Quinolinemethanol

https://huagongshe.com/ko/reaction/333752

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물7-MethylquinolineHCID 11927—
반응물N-bromobutanimideHCID 67184—
용매Ethyl AcetateHCID 8857—
생성물7-QuinolinemethanolHCID 976093%

반응 단계

To a solution of 7-methylquinoline (2.86 g) in ethyl acetate (100 mL) were added N-bromosuccinimide (3.56 g) and 2,2′-azobis(isobutyronitrile) (197 mg) at room temperature, and the mixture was refluxed for 1.5 hr. The reaction mixture was allowed to cool to room temperature, and washed with water. The obtained organic layer was concentrated under reduced pressure, to the residue were added DME (200 mL), water (100 mL), and silver carbonate (27.6 g), and the mixture was stirred at room temperature for 20 hr. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/methanol), and then purified by NH silica gel column chromatography (ethyl acetate/hexane) to give the title compound (94 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883788B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-4687f1df1c0448c09811688c8d7dd398
출처 메모uspto-grants-2014_11