Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,2,3,4-Tetrahydro-1,1,2,3,4,4,6,7-octamethylnaphthalene | HCID 14446271 | — |
| Product | HCID 14446273 | HCID 14446273 | — |
Reaction Steps
To prepare the corresponding 6-carboxaldehyde, 16 portions of Ce(NH4)2 (NO3)6 (16×16.0 g=256.0 g) in methanol (16×100 ml) is added to a solution of 1,1,2,3,4,4,6,7-octamethyl-1,2,3,4-tetrahydronaphthalene (16.0 g) in methanol (700 ml), over 8 hrs, while maintaining the temperature at 50° C. After about 1/2 of the methanol is evaporated, the resulting product is extracted with petroleum ether 30° C.-50° C./saturated NaCl. After crystallizing in ethanol, treating the mother liquors and recrystallizing, the desired 6-carboxaldehyde, 6-formyl-1,1,2,3,4,4,7-heptamethyl-1,2,3,4-tetrahydronaphthalene is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05292719 |
|---|
| Source dataset | uspto-grants-1994_03 |
|---|
| ORD ID | ord-a6b569ce02c7481fb2fcace0be910378 |
|---|
| Source note | uspto-grants-1994_03 |
|---|