Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 76782947 | HCID 76782947 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 75079484 | HCID 75079484 | 83% |
Reaction Steps
A solution of 1-ethynyl-2,5,5,8a-tetramethyl-1,2,3,5,6,7,8,8a-octahydro-1-naphthalenol (4.00 g; 17.2 mmol) in o-xylene (60 ml) was treated with [V2O6SiPh2]n, (400 mg) [Tetrahedron Lett. 1976, 17, 2981] and heated at reflux (145° C.). After 17 hours, the rearrangement was completed. The reaction mixture was poured into 5% aqueous NaOH. The product was extracted twice with Et2O and washed successively with H2O and twice with satured aqueous NaCl, dried (Na2SO4) and evaporated. Bulb-to-bulb distillation (125° C. (oven temp.)/0.04 mbar) afforded 97% pure (2,5,5,8a-tetramethyl-3,5,6,7,8,8a-hexahydro-1-naphthalenyl)acetaldehyde (3.42 g; yield=83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08227630B2 |
|---|
| Source dataset | uspto-grants-2012_07 |
|---|
| ORD ID | ord-ab6baa3e3eba4619b886ca657cbfa88c |
|---|
| Source note | uspto-grants-2012_07 |
|---|