9-(Phenylmethyl)-9-azabicyclo[3.3.1]nonan-3-one oxime → 9-Benzyl-9-azabicyclo[3.3.1]nonan-3-amine

HRID 463704Notes

Reaction equation

HRID 463704 reaction equation
[CH2:1]([N:8]1[CH:13]2[CH2:14][CH2:15][CH2:16][CH:9]1[CH2:10][C:11](=[N:17]O)[CH2:12]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(O)C.[Ni]>[NH2:17][CH:11]1[CH2:10][CH:9]2[N:8]([CH2:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[CH:13]([CH2:14][CH2:15][CH2:16]2)[CH2:12]1

Participants

4

Reactant 1

HCID 28225629-(Phenylmethyl)-9-azabicyclo[3.3.1]nonan-3-one oxime

Product 1

HCID 131787589-Benzyl-9-azabicyclo[3.3.1]nonan-3-amineYield 61%

Reagents, catalysts & solvents 2

HCID 935NickelCatalystHCID 702EthanolSolvent

Procedure

9-Benzyl-9-azabicyclo-(3.3.1)-nonan-3-one oxime (4.0 g; 0.0164 mole), m.p. 134°, was dissolved in ethanol (100 ml) and hydrogenated at 50°-60° at 250 psi in the presence of Raney nickel. The mixture was filtered after 24 hours through kieselguhr and evaporated in vacuo. The reulting oil was dissolved in dilute hydrochloric acid (50 ml) extracted with ethyl acetate (3×150 ml), the aqueous layer was basified and re-extracted with ethyl acetate (3×150 ml). The combined organic extracts were dried (K2CO3), filtered and evaporated in vacuo to yield 3-amino-9-benzyl-9-azabicyclo-[3,3,1]-nonane (2.3 g; 61%), used without further purification.

Workup

  1. filtrationThe mixture was filtered after 24 hours through kieselguhr
  2. customevaporated in vacuo
  3. dissolutionThe reulting oil was dissolved in dilute hydrochloric acid (50 ml)
  4. extractionextracted with ethyl acetate (3×150 ml)
  5. extractionre-extracted with ethyl acetate (3×150 ml)
  6. dry with materialThe combined organic extracts were dried (K2CO3)
  7. filtrationfiltered
  8. customevaporated in vacuo

Sources & evidence

ORD record
ord-fbcd09d2518e4f4b97bbfd22256660ca
Source dataset
uspto-grants-1985_10
Patent number
US04544660

Reaction notes

Loading…