Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 2,6-Dimethyl 1,7-octadiene | HCID 522313 | — |
| Reactant | HCID 11308239 | HCID 11308239 | — |
| Reactant | Acetic acid--water (1/1) | HCID 21899381 | — |
| Product | HCID 19973343 | HCID 19973343 | 41% |
Reaction Steps
A 5-L pressure reaction vessel was charged with a solution comprising 83.3 mg of Rh(CO)2 (CH3COCHCOCHS3), 20.87 g of tris(2,6-di-t-butylphenyl) phosphite and 500 mL of benzene, and the vessel was pressurized to 90 atm with a mixed gas of carbon monoxide/hydrogen (1/1). After the temperature had been elevated to 100° C., 2.05 kg of 2,6-dimethyl-1,7-octadiene was added over a period of 5 hours, during which the pressure was maintained at 90 atm. After completion of the feed, the reaction was continued for a further 5 hours at the same temperature and pressure. The reaction vessel was cooled and then the gas therein was purged. The reaction mixture was taken out and then benzene was distilled off under vacuum. The residue was subjected to simple distillation to remove the catalytic components. The resulting distillate was rectified to give 3,7-dimethyldecanedial as an almost colorless liquid having a boiling point of 99° to 100° C. at 0.85 mmHg. The yield was 41% (1.20 kg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05606005 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-0eba06100b44493c80bb831b40971cca |
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| Source note | uspto-grants-1997_02 |
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