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HRID 587914作成日:2026年10月26日

1,3-Dibromopropane → 5-Bromo-2-(3,4-dimethoxyphenyl)-2-isopropylpentanenitrile

https://huagongshe.com/reaction/587914

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-DibromopropaneHCID 8001—
反応物Ammonium ChlorideHCID 25517—
反応物2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrileHCID 89396—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
溶媒TetrahydrofuranHCID 8028—
生成物5-Bromo-2-(3,4-dimethoxyphenyl)-2-isopropylpentanenitrileHCID 13535571—

反応条件

温度-30 °C

反応手順

To a solution of 11.21 g (51.1 mmol) of 2-(3,4-dimethoxyphenyl)-3-methylbutanenitrile in 126 mL of tetrahydrofuran (THF) at −30° C., was slowly added 46.0 mL (46.0 mmol) of sodium bis(trimethylsilyl)amide (NaHMDS, 1.0 M in THF). The mixture was stirred at −30° C. for 10 minutes and 9.40 mL (256 mmol) of 1,3-dibromopropane was added dropwise. The mixture was warmed to 22° C. and stirred for about 16 h. A saturated aqueous solution of NH4Cl was then added and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried (Na2SO4), filtered and evaporated. The residue was purified by flash chromatography on silica gel eluting first with hexane and then gradually increasing to 15% ethyl acetate/hexane to give 5-bromo-2-(3,4-dimethoxyphenyl)-2-isopropylpentanenitrile as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09227918B2
出典データセットuspto-grants-2016_01
ORD IDord-10e46017d7674332baeb174f1751786b
出典メモuspto-grants-2016_01