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HRID 587913作成日:2026年10月24日

2-Bromopropane → 2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrile

https://huagongshe.com/ja/reaction/587913

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromopropaneHCID 6358—
反応物Ammonium ChlorideHCID 25517—
反応物3,4-DimethoxybenzeneacetonitrileHCID 66727—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
溶媒TetrahydrofuranHCID 8028—
生成物2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrileHCID 89396—

反応条件

温度-30 °C

反応手順

To a solution of 9.99 g (56.4 mmol) of (3,4-Dimethoxyphenyl)acetonitrile in 141 mL of tetrahydrofuran (THF) at −30° C., was slowly added 56.4 mL (56.4 mmol) of sodium bis(trimethylsilyl)amide (NaHMDS, 1.0 M in THF). The mixture was stirred at −30° C. for 10 minutes and 10.6 mL (113.0 mmol) of 2-bromopropane was added. The mixture was heated to reflux for 2 hours (h) then left at 22° C. for about 16 h. A saturated aqueous solution of NH4Cl was 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 2-(3,4-dimethoxyphenyl)-3-methylbutanenitrile 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-1de0264fd88043fa95c95fd18dd6fde3
出典メモuspto-grants-2016_01