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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892665Generated: October 25, 2026

Oxygen → Ethyl 2,6-dimethyl-8-oxoocta-2,4,6-trienoate

https://huagongshe.com/reaction/892665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantSodium ChlorideHCID 5234—
Reactant2,2,6,6-Tetramethyl-piperidine 1-oxideHCID 10125083—
ReactantEthyl 8-hydroxy-2,6-dimethylocta-2,4,6-trien-1-oateHCID 54365984—
CatalystCuprous chlorideHCID 62652—
SolventDimethylformamideHCID 6228—
ProductEthyl 2,6-dimethyl-8-oxoocta-2,4,6-trienoateHCID 5342389792%

Reaction Steps

From 50 to 60 ml of oxygen per minute were passed through a solution of 30.0 g (142.7 millimoles) of ethyl 8-hydroxy-2,6-dimethylocta-2,4,6-trien-1-oate (isomer mixture) and 2.23 g (14.3 millimoles) of 2,2,6,6-tetramethylpiperidine 1-oxide in 75 ml of N,N-dimethylformamide, after the addition of 1.42 g (14.3 millimoles) of copper(I) chloride, the temperature being kept at from 20° to 35° C. with the aid of an ice bath. After 1 hour, the mixture was poured onto 150 ml of aqueous sodium chloride solution and extracted with methyl tert-butyl ether. The organic phase was first washed with a solution of sodium iodide in 5% strength hydrochloric acid, shaken with aqueous sodium thiosulfate solution, washed with water and then dried over sodium sulfate, after which the solvent was removed under reduced pressure. 27.3 g (92% yield) of ethyl 2,6-dimethyl-8-oxoocta-2,4,6-trien-1-oate were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05118866
Source datasetuspto-grants-1992_06
ORD IDord-6519517ed07d47a7ae0061ba9fee6374
Source noteuspto-grants-1992_06