Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4,8-Cyclododecadien-1-one | HCID 601176 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | Cyclododecanone | HCID 13246 | — |
Reaction Steps
In a reactor battery consisting of a tubular reactor with liquid circuit and a postreactor, cyclododeca-4,8-dien-1-one was hydrogenated continuously (30 bar, temperatures 130°, each reactor in trickle mode, catalyst 0.2% Pd on alumina), which also comprised approx. 0.5% polyunsaturated C12-aldehydes. The entire amount of hydrogen (2.1 molar equivalents based on reactant, i.e. 5 mol % hydrogen excess) was introduced into the main reactor and transferred together with the product stream into the postreactor. Downstream of the postreactor, the residual gas was discharged as offgas. At a total catalyst hourly space velocity of 0.5 kg of dienone/liter of catalyst×h, the conversion was 99.8%, i.e. the reaction effluent still contained 0.2% of unconverted olefin. In a subsequent distillation, it was possible to obtain cyclododecanone in a purity of 99.4%; 0.2% of unsaturated cyclododecanone was undesired secondary constituent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754925B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-b1d439a4a7f94c458e9164f7774b2b82 |
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| Source note | uspto-grants-2010_07 |
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