Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Isobutyl ketone | HCID 7958 | — |
| Product | Mesityl oxide | HCID 8858 | 2% |
Reaction Steps
Per hour, 1.5 liters of acetone were passed by the trickle method, i.e. from above, through this tubular reactor, which was at 150° C. and under a hydrogen pressure of 25 bar. This speed corresponds to a mean residence time of about 2 hours, within which an acetone conversion of 38% was achieved. The yield of 4-methylpentan-2-one, based on material converted, was 91%; in addition, 1% of isopropanol, 3% of the double-sided aldolization product 2,6-dimethylheptan-4-one and 2% of 4-methylpent-3-en-2-one were formed. Since the last-mentioned compound is an intermediate of 4-methylpentan-2-one and can be recycled to the synthesis reaction, in order to undergo hydrogenation, the yield of desired products totalled 92%. The conversion and yields were determined by gas chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04270006 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-b456bb9702354f7f85a829512bd3216c |
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| Source note | uspto-grants-1981_05 |
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