Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | HCID 66974043 | HCID 66974043 | — |
| Catalyst | Methanesulfonic Acid | HCID 6395 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66974036 | HCID 66974036 | 25.4% |
Reaction Steps
Hydrochloric acid (HCl, 6 g) was added to a solution of 1,4-dimethyl-bicyclo[3.2.1]octan-3-one (400 g, 2.6 mol, obtained as above in EXAMPLE III), trimethylorthoformate (HC(OCH3)3, 280 g, 2.6 mol), and methanol (CH3OH, 400 mL). The reaction mixture was aged for 3 hours and subsequently quenched with a NaOH solution. Allyl alcohol (CH2CHCH2OH, 300 g, 5.2 mol), acetic acid (CH3COOH, 50 g), and methanesulfonic acid (CH3SO2OH, MSA, 5 g) were added and aged at reflux. The volatile ingredients were distilled off with a Dean Stark trap. The resulting mixture was washed with a Na2CO3 solution. Fractional distillation of the organic layer provided 4-allyl-1,4-dimethyl-bicyclo[3.2.1]octan-3-one (127 g) having a boiling point of 64° C. at a pressure of 0.2 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399522B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-1cbfe91d2958494dbe8f8c3c9d072c09 |
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| Source note | uspto-grants-2013_03 |
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