Hydrochloric Acid → HCID 15284546, compound
Reaction equation
[CH3:1][C:2]1([CH3:20])[C:6]2(OCC[O:7]2)[CH2:5][N:4]([C@@H:11]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH3:12])[C:3]1=[O:19].Cl.C1(C)C=CC(S(O)(=O)=O)=CC=1>CC(C)=O>[CH3:20][C:2]1([CH3:1])[C:6](=[O:7])[CH2:5][N:4]([C@@H:11]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH3:12])[C:3]1=[O:19]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 18.23 g of 9,9-dimethyl-8-oxo-7-[1-(R)-phenylethyl]-7-aza-1,4-dioxaspiro[4.4]nonane, 70 ml of 1N hydrochloric acid and 20 g of p-toluenesulfonic acid in 250 ml of acetone was heated under reflux for 20 hrs. During the reaction, 20 g of p-toluenesulfonic acid was further added. Solvent was removed under reduced pressure and the residue was extracted with chloroform. The extract was washed with a saturated sodium bicarbonate aqueous solution and dried. Solvent was removed under reduced pressure, and the residue was purified by silica gel chromatography (300 g of silica gel in a column) while eluting with a mixture of n-hexane and ethyl acetate (4:1, v/v) to yield 11.85 g a of the titled compound.
Workup
- temperaturewas heated
- temperatureunder reflux for 20 hrs
- additionwas further added
- customSolvent was removed under reduced pressure
- extractionthe residue was extracted with chloroform
- washThe extract was washed with a saturated sodium bicarbonate aqueous solution
- customdried
- customSolvent was removed under reduced pressure
- customthe residue was purified by silica gel chromatography (300 g of silica gel in a column)
- washwhile eluting with a mixture of n-hexane and ethyl acetate (4:1
Sources & evidence
- ORD record
- ord-d7209a94cf2c492aaeeb9df3fa52658b
- Source dataset
- uspto-grants-2000_02
- Patent number
- US06031102
Reaction notes
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