Potassium sodium tartarate → 1beta-Methyl-5-androstene-3beta,17beta-diol
Reaction equation
[CH3:1][C@H:2]1[C@@:19]2([CH3:20])[C:6](=[CH:7][CH2:8][C@@H:9]3[C@@H:18]2[CH2:17][CH2:16][C@@:14]2([CH3:15])[C@H:10]3[CH2:11][CH2:12][C:13]2=[O:21])[CH2:5][C:4](=[O:22])[CH2:3]1.[H-].C(O[Al](OC(C)(C)C)OC(C)(C)C)(C)(C)C.[Li+].C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[K+]>O1CCCC1>[CH3:1][C@H:2]1[C@@:19]2([CH3:20])[C:6](=[CH:7][CH2:8][C@@H:9]3[C@@H:18]2[CH2:17][CH2:16][C@@:14]2([CH3:15])[C@H:10]3[CH2:11][CH2:12][C@@H:13]2[OH:21])[CH2:5][C@@H:4]([OH:22])[CH2:3]1Participants
5
Procedure
A tetrahydrofuran solution of 1β-methyl-5-androstene-3,17-dione is added under nitrogen to a solution of lithium tri-t-butoxyaluminum hydride in tetrahydrofuran. After stirring at room temperature for a period of 18 hours, an aqueous solution of potassium sodium tartrate is added with stirring to form a readily filterable white solid. The reaction mixture is filtered, the filtrate dried over magnesium sulfate, and the solvent removed. The residue is crystallized from an acetone-hexane solution to yield 1β-methyl-5-androstene-3β,17β-diol.
Workup
- stirringwith stirring
- customto form a readily filterable white solid
- filtrationThe reaction mixture is filtered
- dry with materialthe filtrate dried over magnesium sulfate
- customthe solvent removed
- customThe residue is crystallized from an acetone-hexane solution
Sources & evidence
- ORD record
- ord-f132401f8fbf4e15b36062858ee27c62
- Source dataset
- uspto-grants-1978_05
- Patent number
- US04087524
Reaction notes
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