Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Undecane | HCID 14257 | — |
| Reactant | Red-Al | HCID 16684438 | — |
| Reactant | HCID 66974036 | HCID 66974036 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66974041 | HCID 66974041 | 100% |
Reaction Steps
Preparation of 2,4,8-Trimethyl-5-oxa-tricyclo[6.2.1.0*2,6]undecane (Structure 4): 4-Allyl-1,4-dimethyl-bicyclo[3.2.1]octan-3-one (288 g, 1.5 mol, obtained as above in EXAMPLE IV) was added to a solution of Red-Al (65%, 506 g, 1.5 mol) in toluene at 75° C. The reaction mixture was aged for 3 hours while the temperature was maintained at 75° C., then cooled to room temperature, and subsequently quenched with a solution of sodium bicarbonate (NaHCO3). Distillation of the organic layer provided 4-allyl-1,4-dimethyl-bicyclo[3.2.1]octan-3-ol (288 g, 1.5 mol), which was then added to a MSA solution (30 g) in toluene (500 mL) and heated to reflux for 3 hours. The reaction mixture was subsequently washed with a Na2CO3 solution. Fractional distillation of the organic layer provided 2,4,8-trimethyl-5-oxa-tricyclo[6.2.1.0*2,6*]undecane (170 g) having a boiling point of 62° C. at a pressure of 0.3 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357358B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-fa5560a3480843a5890d2fc0df1c01a4 |
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| Source note | uspto-grants-2013_01 |
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