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HRID 587913생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물2-BromopropaneHCID 6358—
반응물Ammonium ChlorideHCID 25517—
반응물3,4-DimethoxybenzeneacetonitrileHCID 66727—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
용매TetrahydrofuranHCID 8028—
생성물2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrileHCID 89396—

반응 조건

온도-30 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09227918B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-1de0264fd88043fa95c95fd18dd6fde3
출처 메모uspto-grants-2016_01