Ethyl Acetate → HCID 86758842, compound
Reaction equation
[H-].[Na+].[CH3:3][N:4]1[CH2:10][CH:9]2[C:11](=O)[CH:6]([C@H:7]([CH3:14])[C@H:8]2[CH3:13])[CH2:5]1.[C:15]([O:18][CH2:19][CH3:20])(=[O:17])[CH3:16]>O1CCCC1>[CH3:3][N:4]1[CH2:10][CH:9]2[C:11](=[CH:16][C:15]([O:18][CH2:19][CH3:20])=[O:17])[CH:6]([C@H:7]([CH3:14])[C@H:8]2[CH3:13])[CH2:5]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
To a solution of 4.35 g of triethyl phosphonoacetate in tetrahydrofuran (50 ml) was added 0.85 g of sodium hydride (oily: 60-72%) under ice-cooling and the resulting mixture was stirred at 0° C. for 10 minutes. Then a solution of 2.7 g of the crude (6R*,7R*)-3,6,7-trimethyl-3-azabicyclo[3.2.1]octan-8-one in tetrahydrofuran (20 ml) was added thereto and the reaction mixture was heated under reflux for 1 hour. After adding ethyl acetate, the reaction mixture was washed with a saturated aqueous solution of sodium chloride and the organic layer was dried over anhydrous magnesium sulfate. After distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (eluted with n-hexane/ethyl acetate) to thereby give 1.6 g of the title compound as a pale yellow oily substance.
Workup
- temperaturecooling
- temperaturethe reaction mixture was heated
- temperatureunder reflux for 1 hour
- washthe reaction mixture was washed with a saturated aqueous solution of sodium chloride
- dry with materialthe organic layer was dried over anhydrous magnesium sulfate
- distillationAfter distilling off the solvent under reduced pressure
- customthe residue was purified by silica gel column chromatography (eluted with n-hexane/ethyl acetate)
Sources & evidence
- ORD record
- ord-762f92867a8c4f01a81022eab6ecd2ce
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06518423B1
Reaction notes
Loading…