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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1368224생성일: 2026년 10월 27일

N-bromobutanimide → 4-Acetoxy-2-chlorobenzylbromide

https://huagongshe.com/reaction/1368224

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물Phenol, 3-chloro-4-methyl-, acetateHCID 538898—
촉매2,2'-Azobis(2,4-dimethyl-4-methoxyvaleronitrile)HCID 85867—
용매Carbon TetrachlorideHCID 5943—
생성물4-Acetoxy-2-chlorobenzylbromideHCID 2238791159.2%

반응 단계

To a solution of 4-acetoxy-2-chlorotoluene (13.4 g) in carbon tetrachloride (134 ml) were added N-bromosuccinimide (12.9 g) and 2,2′-azobis(4-methoxy-2,4-dimethylvaleronitrile) (1.12 g), and the mixture was refluxed under heating for 2.5 hr. The reaction mixture was concentrated to dryness under reduced pressure. To the residue was added hexane (270 ml) and the mixture was stirred at room temperature for 10 min. The insoluble matter was filtered off and washed with hexane. The filtrate and washing were combined and washed 3 times with saturated aqueous sodium hydrogen carbonate solution and once with saturated brine. The organic layer was dried over magnesium sulfate and concentrated to dryness under reduced pressure. The residue was crystallized from hexane to give 4-acetoxy-2-chlorobenzylbromide as colorless crystals (11.3 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06573274B1
출처 데이터셋uspto-grants-2003_06
ORD IDord-643eb67536bd4463b2be2b975b623111
출처 메모uspto-grants-2003_06