참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,3-Dibromopropane | HCID 8001 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 2-(3,4-Dimethoxyphenyl)-3-methylbutanenitrile | HCID 89396 | — |
| 반응물 | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Bromo-2-(3,4-dimethoxyphenyl)-2-isopropylpentanenitrile | HCID 13535571 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09227918B2 |
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| 출처 데이터셋 | uspto-grants-2016_01 |
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| ORD ID | ord-10e46017d7674332baeb174f1751786b |
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| 출처 메모 | uspto-grants-2016_01 |
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