Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | HCID 86739790 | HCID 86739790 | — |
| Catalyst | HCID 53249311 | HCID 53249311 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86739789 | HCID 86739789 | — |
Reaction Steps
100 g of limonenemonoaldehyde (4-methylcyclohex-3-ene-β-methylpropanal), 300 ml of cyclohexane and 0.1 g of dimeric rhodium carbonyl-chloride were introduced into a stainless steel autoclave of 700 ml capacity and were heated to 145° C. under water gas (CO/H2), while stirring. The pressure was kept between 200 and 220 bar by regularly forcing in more water gas. After 2 hours, the pressure remained constant. The autoclave was cooled and let down and the reaction mixture was separated into its components by thin film distillation. 75 g of limonenedialdehyde (4-methyl-3-formylcyclohexane-β-methylpropanal) were obtained at 150° C. under 0.05 mbar, corresponding to a selectivity of 75%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04487966 |
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| Source dataset | uspto-grants-1984_12 |
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| ORD ID | ord-e4650ecadc294dc9a8b0f6f9d6a54bc2 |
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| Source note | uspto-grants-1984_12 |
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