Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Bromobutane | HCID 6554 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Product | 5-Methyl-2-hepten-4-ol | HCID 54181019 | — |
| Product | HCID 178456030 | HCID 178456030 | — |
Reaction Steps
2-Butylmagnesium bromide is prepared from 24.32 g of magnesium filings and 137 g of 2-bromobutane in 100 ml of ether. 56 g of crotonaldehyde dissolved in 60 ml of ether are added dropwise to the solution at 0° to 10° C. The mixture is then boiled for 2 hours under reflux temperature. Thereafter it is cooled, the batch decomposed with ice water/hydrochloric acid and the product extracted, neutralized and distilled. 56 g of 5-methyl-hept-2-en-4-ol of boiling point 70° C./18 mb are obtained. To 52 g of this alcohol there is slowly added a mixture of 40.34 g of sodium dichromate and 54.1 g of sulphuric acid, while cooling with ice. After a further hour's reaction at room temperature, the batch is extracted with ether, the organic phase is washed until neutral, the solvent stripped off and the crude product distilled. Redistillation using a slotted tube column gives 17.2 g of 5-methyl-hept-2-en-4-one of boiling point 72° C./20 mb.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04563365 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-33d833bb18e341b188b1a474592984e9 |
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| Source note | uspto-grants-1986_01 |
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