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HRID 2181016作成日:2026年10月27日

N-bromobutanimide → 4-Acetoxy-2-chlorobenzylbromide

https://huagongshe.com/reaction/2181016

反応式

関与物質

役割名称HCID仕込み量
反応物N-bromobutanimideHCID 67184—
反応物Phenol, 3-chloro-4-methyl-, acetateHCID 538898—
触媒2,2'-Azobis(2,4-dimethyl-4-methoxyvaleronitrile)HCID 85867—
溶媒Carbon TetrachlorideHCID 5943—
生成物4-Acetoxy-2-chlorobenzylbromideHCID 2238791159.2%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06890934B2
出典データセットuspto-grants-2005_05
ORD IDord-6cdca5b2001c434a91355d577af538b2
出典メモuspto-grants-2005_05