HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isobutyl Ketone → Isobutyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Cobalt dibromide | HCID 24610 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Isobutyl ketone | HCID 7958 | — |
| Product | 2-Heptanone | HCID 8051 | — |
| Product | Mesityl oxide | HCID 8858 | — |
Reaction Steps
10 g of acetone, 2 g of cobalt bromide (CoBr.6H2O), 2 g of triphenylphosphine and 5 g of N-methyl-2-pyrrolidone were added to a shaking-type, stainless steel autoclave having a net capacity of 100 ml, and a mixed gas of hydrogen and carbon monoxide (molar ratio of H2 /CO=1) were introduced thereto under a pressure of 180 kg/cm2 gage, and reaction was carried out at 250° C. for two hours. As a result, a selectivity to methylisobutylketone of 75% was obtained with an acetone conversion of 48.6% by mole. In addition, isopropanol, methylpentylketone, diisobutylketone, mesityl oxide, etc. were formed as by-products.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04289911 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-4c7af55546f54e7583d29b9fd21272ff |
| Source note | uspto-grants-1981_09 |