Water → 17-Methylenestra-1,3,5(10)-trien-3-yl methyl ether
Reaction equation
[CH2:1]=[C:2]1[CH2:7][CH2:6][C@H:5]2[C@H:8]3[C@H:17]([CH2:18][CH2:19][C@:3]12[CH3:4])[C:16]1[CH:15]=[CH:14][C:13]([OH:20])=[CH:12][C:11]=1[CH2:10][CH2:9]3.[C:21](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O.O>C(O)C>[CH3:21][O:20][C:13]1[CH:14]=[CH:15][C:16]2[C@@H:17]3[C@H:8]([C@H:5]4[C@@:3]([CH2:19][CH2:18]3)([CH3:4])[C:2](=[CH2:1])[CH2:7][CH2:6]4)[CH2:9][CH2:10][C:11]=2[CH:12]=1Participants
Procedure
To a stirred suspension of 17-methylenestra-1,3,5(10)-trien-3-ol (5.37 g, 20.0 mmol) and potassium carbonate (50.82 g, 0.3678 mol) at reflux in 90% ethanol (500 ml) was added dimethyl sulfate (5.0 ml, 53 mmol). After 1/2 h reflux additional dimethyl sulfate (36 ml, 0.38 mol, in three 12 ml aliquots) was added over the period of 1 h. See FIG. 160. The reaction was refluxed a further hour, following which 360 ml of water were added and the mixture was placed in the refrigerator overnight. The resulting suspension was filtered and washed with 80 ml of 60% methanol+three 80 ml portions of 5% (w/w) sodium hydroxide+three 80 ml portions of water. The residue was recrystallized from aqueous methanol to give white crystals (3.88 g, 13.7 mmol, 69%), m.p. 59-62° C. TLC (20% ethyl acetate/hexanes on silica gel) showed product (Rf 0.63) with trace contaminants at Rf 0.37 and at the origin.
Workup
- additionwas added over the period of 1 h
- temperatureThe reaction was refluxed a further hour
- additionwere added
- customwas placed in the refrigerator overnight
- filtrationThe resulting suspension was filtered
- washwashed with 80 ml of 60% methanol+three 80 ml portions of 5% (w/w) sodium hydroxide+three 80 ml portions of water
- customThe residue was recrystallized from aqueous methanol
Sources & evidence
- ORD record
- ord-8d27777a38724442a3b5f8b535aecf35
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06057439
Reaction notes
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