Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | 1-Bromopentane | HCID 8057 | — |
| Edukt | 4-Chlorobutyronitrile | HCID 12336 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Produkt | 1-Chlorononan-4-one | HCID 20386103 | — |
Reaktionsschritte
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 (100 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° /14 mm.; pmr (CDCl3) δ 0.90 (3H,t), 3.56 (2H,t,CH 2 Cl).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04091107 |
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| Quelldatensatz | uspto-grants-1978_05 |
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| ORD ID | ord-c7ad9e740cfa4668b3f1745af9eda0e9 |
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| Quellennotiz | uspto-grants-1978_05 |
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