![](/StructureFile/ChemBookStructure9/GIF/CB6416023.gif)
9-AZABICYCLO[3,3,1]NONYL-3-ENDO-OL synthesis
- Product Name:9-AZABICYCLO[3,3,1]NONYL-3-ENDO-OL
- CAS Number:504-12-1
- Molecular formula:C8H15NO
- Molecular Weight:141.21
![9-azabicyclo[3.3.1]nonan-3-one](/CAS/GIF/4390-39-0.gif)
4390-39-0
48 suppliers
$88.00/250mg
![9-AZABICYCLO[3,3,1]NONYL-3-ENDO-OL](/StructureFile/ChemBookStructure9/GIF/CB6416023.gif)
504-12-1
27 suppliers
$580.00/1g
![9-Azabicyclo[3.3.1]nonan-3-ol](/CAS/20150408/GIF/26651-94-5.gif)
26651-94-5
12 suppliers
inquiry
Yield:98 % ee
Reaction Conditions:
with cis-RuCl2[dppb][Me-bima];potassium tert-butylate;hydrogen in butan-1-ol at 25; under 7600.51 Torr; for 17 h;Overall yield = 99 %;Time;Reagent/catalyst;Concentration;Solvent;
Steps:
6 Example 6 Preparation Examples of endo-9-azabicyclo[3.3.1]nonan-3-ol
Example 6
Preparation Examples of endo-9-azabicyclo[3.3.1]nonan-3-ol
A reduction reaction of a 9-azabicyclo[3.3.1]nonan-3-one was conducted using a cis-RuCl2(dppb)(ammp) or a cis-RuCl2(Me-bima) under the conditions shown in Table 6.
The results are shown in Table 6.
References:
US2016/200726,2016,A1 Location in patent:Paragraph 0110
![9-Azabicyclo[3.3.1]nonan-3-ol, 9-(phenylmethyl)-, endo-](/CAS/20180601/GIF/70243-51-5.gif)
70243-51-5
22 suppliers
inquiry
![9-AZABICYCLO[3,3,1]NONYL-3-ENDO-OL](/StructureFile/ChemBookStructure9/GIF/CB6416023.gif)
504-12-1
27 suppliers
$580.00/1g
![9-Methyl-9-azabicyclo[3.3.1]nonan-3-one](/CAS/GIF/552-70-5.gif)
552-70-5
138 suppliers
$21.00/250mg
![9-AZABICYCLO[3,3,1]NONYL-3-ENDO-OL](/StructureFile/ChemBookStructure9/GIF/CB6416023.gif)
504-12-1
27 suppliers
$580.00/1g