Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 22562217 | HCID 22562217 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | HCID 11184346 | HCID 11184346 | 72% |
Reaction Steps
To 3.80 g (11.1 mmol) 8-benzyl-3-naphthalen-2-yl-8-aza-bicyclo[3.2.1]octan-3-ol was added 1.20 g (19.0 mmol) of ammonium formate, 100 mL MeOH, and 2.46 g Pd/C (10 wt. %). The reaction mixture was heated to 50° C., and was monitored by TLC on a SiO2 plate with CHCl3:MeOH (10:1). After 21 h, the mixture was cooled to room temperature, filtered through a pad of celite and evaporated to afford 2.0 g (7.9 mmol, a 72% yield) of the title compound as an off-white solid. MS (ES) m/z: 344 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07381723B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-d45862d990ed48b8a3c6f130428dab5b |
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| Source note | uspto-grants-2008_06 |
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