HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67838128, compound → 2,2,3,6-Tetramethylcyclohex-3-ene-1-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67838128 | HCID 67838128 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2,3,6-Tetramethylcyclohex-3-ene-1-carbaldehyde | HCID 19896078 | 82% |
Reaction Steps
Prepared according to the method described, starting from 15.0 g (70 mmol) of PCC in 150 ml of CH2Cl2 and 8.38 g (50 mmol) of cis-2,2,3,6-tetramethyl-3-cyclohexene-1-methanol, obtained as in example 3b., in 50 ml of CH2Cl2. After stirring for 1 h, the reaction mixture was treated as described above to yield 6.77 g of the desired aldehyde in the form of a yellow oil (2 isomers, cis/trans~9:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05118865 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-7ba4cea5b60a4a8695a6daee5abe54ca |
| Source note | uspto-grants-1992_06 |