참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | 1-Bromopentane | HCID 8057 | — |
| 반응물 | 4-Chlorobutyronitrile | HCID 12336 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 생성물 | 1-Chlorononan-4-one | HCID 20386103 | — |
반응 단계
To the Grignard reagent prepared from a mixture of amyl bromide (226.59 g.; 1.5 moles) and magnesium (36.48 g.; 1.5 moles) in ether (1000 ml.) is added, dropwise, during one hour, 4-chlorobutyronitrile (155.34 g.; 1.5 moles). Stirring is continued for an additional one hour. The reaction mixture is poured into a mixture of finely crushed ice (1000 g.) and concentrated hydrochloric acid (750 ml.). The ether layer is separated quickly and discarded. The aqueous layer is heated on a steam bath for one hour to hydrolyze the intermediate imine and cause the separation of the ketone as an oil. After cooling, the oil is extracted with ether and the combined extracts are washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent is removed under vacuum and the residual oil is distilled to give 69.0 g. (26%) of colorless oil, b.p. 115°-117° C./14 mm.; pmr (CDCl3) δ 0.090 (3H,t), 3.56 (2H,t,CH2Cl).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04175203 |
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| 출처 데이터셋 | uspto-grants-1979_11 |
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| ORD ID | ord-a0aa2a6d84ee47cc9acefa3def131aec |
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| 출처 메모 | uspto-grants-1979_11 |
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