HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411517Generated: October 30, 2026
Sodium Hydroxide → 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine
https://huagongshe.com/reaction/411517
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 3-Benzyl-3-azabicyclo(3.2.1)octan-8-one | HCID 15639134 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine | HCID 18541030 | 49% |
Reaction Steps
A mixture of sodium cyanoborohydride (35.0 g, 0.557 mol) and zinc chloride (37.9 g, 0.278 mol) in methanol (500 mL) was added dropwise to a mechanically stirred mixture of 3-benzyl-3-azabicyclo[3.2.1]octan-8-one (Preparation A; 120 g, 0.557 mol) and methylamine hydrochloride (151 g, 2.23 mol) in methanol (1.0 L) at 25° C. under nitrogen. After 2.5 h of stirring, 6 N NaOH (90 mL) was added dropwise. The mixture was filtered through a pad of Celite®, washing with methanol (500 mL). The filtrate was concentrated in vacuo. Water (500 mL) was added, and the aqueous mixture was extracted with ethyl acetate (3×500 mL). The combined organic extracts were dried (Na2SO4), and concentrated in vacuo. The residue was chromatographed, eluting with methanol dichloromethane (1:10), to afford 63.0 g (49%) of the sub-title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06559162B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-dd20e89bb4d74da892ac2debda183ca5 |
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| Source note | uspto-grants-2003_05 |
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