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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxygen | HCID 977 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 2,2,6,6-Tetramethyl-piperidine 1-oxide | HCID 10125083 | — |
| Reactant | Ethyl 8-hydroxy-2,6-dimethylocta-2,4,6-trien-1-oate | HCID 54365984 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2,6-dimethyl-8-oxoocta-2,4,6-trienoate | HCID 53423897 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05118866 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-6519517ed07d47a7ae0061ba9fee6374 |
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| Source note | uspto-grants-1992_06 |
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