HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,6-Trimethylcyclohexanone → Tetramethyl-cyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,6-Trimethylcyclohexanone | HCID 17000 | — |
| Reactant | 2,2,3,6-Tetramethylcyclohexan-1-ol | HCID 19910535 | — |
| Product | Tetramethyl-cyclohexanone | HCID 22644489 | — |
Reaction Steps
If the procedure of Example 8 is followed but instead of 28 g of 2,2,6-trimethyl-cyclohexanone 31 g of 2,2,3,6-tetramethyl-cyclohexanol are employed, fractional distillation gives 9.6 g of unconverted tetramethyl-cyclohexanone and 21 g (corresponding to 73% of theory, based on ketone converted) of 2,2,3,6-tetramethyl-1-(but-1'-yn-3'-en-1'-yl)-cyclohexanol of boiling point 66°-67° C/0.2 mm Hg and refractive index nD25 = 1.5018. Fragrance note: faintly floral, coniferous, fruity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04088681 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-307b71d4dda84a05a97ec712f46ba46b |
| Source note | uspto-grants-1978_05 |