Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | 3-Methyl-2-butanone | HCID 11251 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | 1188-95-0 | HCID 70915 | — |
| Product | 3,3-Dimethylhex-5-en-2-one | HCID 12604173 | 76% |
Reaction Steps
63.6 g (1 mol) of powdered technical grade potassium hydroxide (88% strength) are suspended in 200 ml of toluene, and 10 g of trioctylammonium chloride are added. A mixture of 76.5 g (1 mol) of allyl chloride and 129 g (1.5 mols) of methyl isopropyl ketone is then added dropwise so that the temperature does not exceed 70° C. The mixture is stirred for a further 4 hours at 70° C., and is worked up as in Example 1. 96 g (76% of theory) of 4,4-dimethylhex-1-en-5-one of the abovementioned boiling point are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04686291 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-51cb3e7d23ad4c4bb41ea2033ba73586 |
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| Source note | uspto-grants-1987_08 |
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