Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 3,5-Dimethylcyclohexanone | HCID 137544 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69885098 | HCID 69885098 | — |
Reaction Steps
To a solution of 180 g of paraformaldehyde in methanol (500 ml) were slowly added under ice-cooling 230 ml of a 40% solution of methylamine in methanol and 17 ml of acetic acid. After adding dropwise a solution of 250 ml of 3,5-dimethylcyclohexanone in methanol (1 l) thereinto, the resulting mixture was heated under reflux for 5 hours. Then the reaction mixture was cooled to room temperature and the solvent was distilled off under reduced pressure. The residue was acidified by adding dilute hydrochloric acid and then extracted with ethyl acetate. The aqueous layer was made basic by adding sodium hydroxide and then extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. Then the residue was distilled under reduced pressure (100-110° C./1 mmHg) to thereby give 79 g of crude (6R*,8R*)-3,6,8-trimethyl-3-azabicyclo[3.3.1]nonan-9-one as a pale yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518423B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-d17775ee410d440ba57534b2ccb943fc |
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| Source note | uspto-grants-2003_02 |
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