HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 8-Methyl-3,8-diazabicyclo(3.2.1)octane dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane dihydrochloride monohydrate | HCID 21545491 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 8-Methyl-3,8-diazabicyclo(3.2.1)octane dihydrochloride | HCID 22120189 | 152.9% |
Reaction Steps
A mixture of 3-benzyl-8-methyl-3,8-diazabicyclo[3.2.1]octane dihydrochloride monohydrate (18.1 g, 0.059 mole) in absolute ethanol (200 ml) and 10% palladium on charcoal (3.0 g) was hydrogenated for 2 hours at atmospheric pressure. Sufficient water was added to dissolve the insoluble hydrochloride salt that had formed, and the reaction was filtered. The filtrate was evaporated in vacuo, the residue was triturated in hot absolute ethanol, and the mixture was filtered to yield 8.98 g of 8-methyl-3,8-diazabicyclo[3.2.1]octane dihydrochloride, melting point 315° C (dec.). The mother liquor was treated with ethanolic dry hydrogen chloride to afford an additional 2.28 g. Yield: 12.26 g (96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03951980 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-f6e3cf663f174dc48486f036354f29ea |
| Source note | uspto-grants-1976_04 |