Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Crotonaldehyde | HCID 447466 | — |
| Edukt | 5-Methyl-2-hepten-4-one (natural) | HCID 517791 | — |
| Edukt | HCID 178456030 | HCID 178456030 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 5-Methyl-2-hepten-4-ol | HCID 54181019 | — |
Reaktionsschritte
5-Methyl-hept-2-en-4-one to be used according to the invention can be obtained for example by reacting 2-butylmagnesium bromide (prepared, for example, from 2-bromobutane and magnesium filings) with crotonaldehyde in ether solution. 5-Methyl-hept-2-en-4-ol is obtained as an intermediate and is oxidized with a mixture of sodium dichromate and sulphuric acid to give 5-methyl-hept-2-en-4-one. The 5-methyl-hept-2-en-4-one is obtained as a mixture of the cis- and trans-isomers, with the latter predominating. The isomer mixture can be separated into the cis-isomer and trans-isomer by simple methods of separation, such as, for example, fractional distillation by a packed column or slotted tube column or preparative gas chromatography. However, it has been found that the use of the individual isomers offers no advantages over the use of the mixture.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04654168 |
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| Quelldatensatz | uspto-grants-1987_03 |
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| ORD ID | ord-59d12fc1e4514907a882ff8d9ed6f989 |
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| Quellennotiz | uspto-grants-1987_03 |
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