Diethyl Ether → 13-Ethyl-17beta-(2-hydroxyethoxy)-3-methoxygona-1,3,5(10)-triene
Reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH2:11]([C@:13]12[CH2:21][CH2:20][C@@H:19]3[C:22]4[CH:23]=[CH:24][C:25]([O:30][CH3:31])=[CH:26][C:27]=4[CH2:28][CH2:29][C@H:18]3[C@@H:17]1[CH2:16][CH2:15][C:14]2=[O:32])[CH3:12].[CH3:33][CH2:34][O:35]CC>S(=O)(=O)(O)O>[CH2:11]([C@:13]12[CH2:21][CH2:20][C@@H:19]3[C:22]4[CH:23]=[CH:24][C:25]([O:30][CH3:31])=[CH:26][C:27]=4[CH2:28][CH2:29][C@H:18]3[C@@H:17]1[CH2:16][CH2:15][C@@H:14]2[O:32][CH2:33][CH2:34][OH:35])[CH3:12]Participants
Procedure
Prepare a solution of ether (100 ml), aluminum chloride (13.3 g) and lithium aluminum hydride (15 ml. of a 1 M solution). Stir for 20 minutes. Add to a cool solution of dl-13-ethyl-3-methoxygona-1,3,5(10)-trien-17-one, cyclic ethylene ketal (17.1 g) in ether (1,000 ml). Stir the reaction mixture and cool in an ice-water bath for 4 hours. Dilute with 2 N sulfuric acid until a clear solution results. Separate the ether layer, wash with saturated sodium bicarbonate solution, and evaporate. Treat the residue with ethanol (200 ml), concentrated hydrochloric acid (5 ml) and water (10 ml) on a steam bath for 30 minutes. Evaporate, then recrystallize from ethanol to obtain dl-13-ethyl-17β-(2-hydroxyethoxy)-3-methoxygona-1,3,5(10)-triene (8.1 g), m.p. 131°-132°; ultraviolet absorption peak at 278 mμ (ε2,130), infrared maximum at 2.93 μ.
Workup
- stirringStir the reaction mixture
- temperaturecool in an ice-water bath for 4 hours
- customresults
- customSeparate the ether layer
- washwash with saturated sodium bicarbonate solution
- customevaporate
- additionTreat the residue with ethanol (200 ml), concentrated hydrochloric acid (5 ml) and water (10 ml) on a steam bath for 30 minutes
- customEvaporate
- customrecrystallize from ethanol
Sources & evidence
- ORD record
- ord-2aa437aa8ea74519972f6658075553ee
- Source dataset
- uspto-grants-1976_05
- Patent number
- US03959322
Reaction notes
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