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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355806Generated: October 27, 2026

4,8-Cyclododecadien-1-one → Cyclododecanone

https://huagongshe.com/reaction/2355806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,8-Cyclododecadien-1-oneHCID 601176—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
ProductCyclododecanoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754925B2
Source datasetuspto-grants-2010_07
ORD IDord-b1d439a4a7f94c458e9164f7774b2b82
Source noteuspto-grants-2010_07