4-Azatricyclo[4.3.1.13,8]undecan-5-one → 4-Azatricyclo[4.3.1.13,8]undecane
Reaction equation
B#B.[CH:3]12[CH2:13][CH:8]3[CH2:9][CH:10]([CH2:12][CH:6]([CH2:7]3)[C:5](=O)[NH:4]1)[CH2:11]2>O1CCCC1.Cl>[CH:3]12[CH2:13][CH:8]3[CH2:9][CH:10]([CH2:12][CH:6]([CH2:7]3)[CH2:5][NH:4]1)[CH2:11]2Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of diborane in tetrahydrofuran (1M, 20 ml) was added dropwise a solution of 2-azatricyclo[4.3.1.14,8 ]-undecan-3-one (1.01 g) in dry tetrahydrofuran (20 ml) under stirring at cooling in an ice-bath. The mixture was stirred under the same condition for 2 hours and then at room temperature overnight. To the reaction mixture was added dropwise IN hydrochloric acid aqueous solution (20 ml). After removal of the solvent under reduced pressure, the residue was washed with ethyl acetate. The aqueous layer was alkalined with IN sodium hydroxide aqueous solution, extracted with ethyl acetate three times and dried over sodium sulfate. Removal of the solvent gave 2-azatricyclo[4.3.1.14,8 ]undecane (0.48 g), which was used in a following reaction step without further purification.
Workup
- temperatureat cooling in an ice-bath
- stirringThe mixture was stirred under the same condition for 2 hours
- customat room temperature
- customovernight
- customAfter removal of the solvent under reduced pressure
- washthe residue was washed with ethyl acetate
- extractionextracted with ethyl acetate three times
- dry with materialdried over sodium sulfate
- customRemoval of the solvent
Sources & evidence
- ORD record
- ord-d302a7cbc83541a1b876d0d135da5dc1
- Source dataset
- uspto-grants-1998_06
- Patent number
- US05763437
Reaction notes
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