Acetone → Dimethyl Ether
Reaction equation
[C:1]([C:4]1[CH:31]=[CH:30][C:7]([O:8][CH2:9][CH2:10][CH2:11][O:12][C:13]2[CH:26]=[CH:25][C:16]3[CH2:17][CH2:18][CH:19]([C:21]([O:23][CH3:24])=[O:22])[O:20][C:15]=3[C:14]=2[CH2:27][CH2:28][CH3:29])=[C:6]([CH2:32][CH2:33][CH3:34])[C:5]=1[OH:35])(=[O:3])[CH3:2].[CH3:36]C(C)=O.C(=O)([O-])[O-].[K+].[K+].CI>O>[CH3:7][O:8][CH3:9].[C:1]([C:4]1[CH:31]=[CH:30][C:7]([O:8][CH2:9][CH2:10][CH2:11][O:12][C:13]2[CH:26]=[CH:25][C:16]3[CH2:17][CH2:18][CH:19]([C:21]([O:23][CH3:24])=[O:22])[O:20][C:15]=3[C:14]=2[CH2:27][CH2:28][CH3:29])=[C:6]([CH2:32][CH2:33][CH3:34])[C:5]=1[O:35][CH3:36])(=[O:3])[CH3:2]Participants
7
Reactant 4
Product 2
Reagents, catalysts & solvents 1
Procedure
Methyl 7-[3-(4-acetyl-3-hydroxy-2-propyl-phenoxy)propoxy]-3,4-dihydro-8-propyl-2H-1-benzopyran-2-carboxylate 493 mg) was added to 25 ml of acetone containing 276 mg of anhydrous potassium carbonate and 282 mg of methyl iodide. The mixture was refluxed for about 24 hours and water was added and the mixture was then extracted with ethyl acetate. The extract was dried, the solvent removed under vacuum, and the residual oil was chromatographed over silica gel with a 40/60 mixture of ethyl acetate/hexane to provide pure methyl ether, methyl 7-[3-(4-acetyl-3-methoxy-2-propylphenoxy)propoxy]-3,4-dihydro-8-propyl-2H-1-benzopyran-2-carboxylate.
Workup
- temperatureThe mixture was refluxed for about 24 hours
- extractionthe mixture was then extracted with ethyl acetate
- customThe extract was dried
- customthe solvent removed under vacuum
- customthe residual oil was chromatographed over silica gel with a 40/60 mixture of ethyl acetate/hexane
Sources & evidence
- ORD record
- ord-f90bdb905ac7449da56fd969bd533971
- Source dataset
- uspto-grants-1994_05
- Patent number
- US05310951
Reaction notes
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