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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250039Generated: October 27, 2026

Alumina → Cyclododecanol

https://huagongshe.com/reaction/1250039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminaHCID 9989226—
ReactantMonoepoxycyclododecadieneHCID 54352584—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
ProductCyclododecanolHCID 1559520%

Reaction Steps

Also, it is known that epoxidized cycloalkanes and/or epoxidized cycloalkenes can be produced by epoxidizing corresponding cycloalkenes with a high yield. If the epoxidized compounds can be converted to corresponding cycloalkanones and cycloalkanols with a high efficiency, the cycloalkanones and the cycloalkanols can be expected to be obtained at a high yield. However, only a small number of reports can be found on methods of converting an epoxidized cycloalkane and/or an epoxidized cycloalkene to a mixture of cycloalkanone with cycloalkanol. For example, J. Mol. Catal., Vol. 69, pages 69 to 103 (1991) discloses a method of hydrogenating a monoepoxycyclododecadiene with hydrogen in the presence of a catalyst comprising palladium carried on a carrier consisting of γ-alumina, under a hydrogen gas pressure of 1.3 MPa at a temperature of 90° C. In this method, cyclododecanol was produced with a yield of 20% or less and no cyclododecanone was produced. When a catalyst comprising palladium carried on a carrier consisting of titania or silica was used in place of the above-mentioned palladium catalyst carried on γ-alumina, the yield of cyclododecanol was low and unsatisfactory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06335472B1
Source datasetuspto-grants-2002_01
ORD IDord-8965c465e8af40daa8c2bb28687f2b49
Source noteuspto-grants-2002_01