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HRID 470724作成日:2026年10月26日

N-bromobutanimide → 1,3-Dibromo-2,4-dimethoxybenzene

https://huagongshe.com/reaction/470724

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2-Bromo-1,3-dimethoxybenzeneHCID 612296—
溶媒AcetonitrileHCID 6342—
生成物1,3-Dibromo-2,4-dimethoxybenzeneHCID 1164505395.1%

反応手順

17.9 g of 1-bromo-2,6-dimethoxybenzene and 200 mL of acetonitrile were placed in a flask, and the resulting mixture was cooled on ice. Then, 14.7 g of N-bromosuccinimide was added. Then, while heating the reaction solution to room temperature, stirring was conducted for 8 hours. 2.39 g of N-bromosuccinimide was further added, and stirring was conducted at room temperature for 7 hours. After completion of the stirring, the solvent was distilled off under reduced pressure. Residues were dissolved in dichloromethane, and washed sequentially with sodium thiosulfate and saturated saline. An organic phase was dried with magnesium sulfate and concentrated. Residues were purified by means of silica gel column chromatography, whereby 23.2 g (yield: 95%) of colorless oil of 1,3-bromo-2,6-dimethoxybenzene was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629430B2
出典データセットuspto-grants-2014_01
ORD IDord-67e35be1c97743f6a2c25e17dc1f599b
出典メモuspto-grants-2014_01