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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744429Generated: October 31, 2026

Oxygen → Cyclododecanol

https://huagongshe.com/reaction/1744429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantCyclododecaneHCID 9268—
ReactantN-HydroxyphthalimideHCID 10665—
CatalystCobalt(II) acetate tetrahydrateHCID 61372—
SolventAcetic AcidHCID 176—
ProductCyclododecanoneHCID 132467.3%
ProductCyclododecanolHCID 1559513.1%

Reaction Steps

In a flask having an internal volume of 100 ml, 8.4 g (50 mmol) of cyclododecane, 4.52 g of acetic acid, 16.3 mg (0.1 mmol) of N-hydroxyphthalimide, 28.9 mg (0.1 mmol) of bis(acetylacetonato)manganese(II) dihydrate, and 2.0 mg (0.01 mmol) of cobalt(II) acetate tetrahydrate were placed, and an oxygen balloon was attached to the reactor. The liquid temperature was raised on an oil bath and was held at 100° C. The reaction was terminated by cooling 6 hours later. A reaction mixture was diluted with 60 g of acetic acid to thereby dissolve all of solid matters. The resulting solution was analyzed to find that a conversion from cyclododecane was 20.6% and a selectivity for dodecanedioic acid was 23.7%. In addition, cyclododecanone (selectivity: 7.3%) and cyclododecanol (selectivity: 13.1%) were by-produced.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015356B2
Source datasetuspto-grants-2006_03
ORD IDord-cb86508fbfa6497bba763938d464c601
Source noteuspto-grants-2006_03