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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744431Generated: November 3, 2026

Oxygen → Cyclododecanol

https://huagongshe.com/reaction/1744431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantCyclododecaneHCID 9268—
ReactantN-HydroxyphthalimideHCID 10665—
CatalystCobalt(II) acetate tetrahydrateHCID 61372—
SolventAcetic AcidHCID 176—
ProductCyclododecanoneHCID 132462.9%
ProductCyclododecanolHCID 155959.8%

Reaction Steps

In a flask having an inner volume of 100 ml, 8.4 g (50 mmol) of cyclododecane, 12.6 g of acetic acid, 32.6 mg (0.2 mmol) of N-hydroxyphthalimide, 57.8 mg (0.2 mmol) of bis(acetylacetonato)manganese(II) dihydrate, and 4.0 mg (0.02 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 4 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 16.1% and a selectivity for dodecanedioic acid was 27.5%. In addition, cyclododecanone (selectivity: 2.9%) and cyclododecanol (selectivity: 9.8%) were by-produced.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015356B2
Source datasetuspto-grants-2006_03
ORD IDord-ddd302ea2b9f45a18bb8dde73699cb43
Source noteuspto-grants-2006_03