HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,3,6-Tetramethylcyclohexanone → 1,2,2,4-Tetramethyl-3-methylene-cyclohexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,3,6-Tetramethylcyclohexanone | HCID 5130444 | — |
| Reactant | 2,2,3,6-Tetramethylcyclohexanecarbaldehyde | HCID 18791057 | — |
| Reactant | 4,4,5,8-Tetramethyl-1-oxaspiro[2.5]octane | HCID 18791059 | — |
| Product | 1,2,2,4-Tetramethyl-3-methylene-cyclohexane | HCID 19915439 | — |
Reaction Steps
The present invention provides a process for the preparation of 4,4,5,8-tetramethyl-1-oxaspiro[2.5]octane which compound can then be converted into useful 2,2,3,6-tetramethyl-cyclohexane-carbaldehyde by treating it with a Lewis type acid. The aldehyde thus obtained possesses a high degree of isomeric purity (equal or higher than 90%). The process of the invention consists in the methylenation of 2,2,3,6-tetramethyl-1-cyclohexanone to give 1,2,2,4-tetramethyl-3-methylene-cyclohexane followed by the epoxidation of the obtained compound to give 4,4,5,8-tetramethyl-1-oxaspiro[2.5]octane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05017711 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-4d719a242553415cbbef42fa9f2764c7 |
| Source note | uspto-grants-1991_05 |