Acetic Acid → 19-Hydroxy-1beta-methyl-4-androsten-3,17-dione

反応式

[OH:1][CH2:2][C@@:3]12[C@@H:20]3[C@H:11]([C@H:12]4[C@@:16]([CH2:18][CH2:19]3)([CH3:17])[C:15](=[O:21])[CH2:14][CH2:13]4)[CH2:10][CH2:9][C:8]1=[CH:7][C:6](=[O:22])[C@H:5]1[CH2:23][C@@H:4]21.C(O)(=O)C>[Zn].C1C=CC=CC=1>[OH:1][CH2:2][C@@:3]12[C@@H:20]3[C@H:11]([C@H:12]4[C@@:16]([CH2:18][CH2:19]3)([CH3:17])[C:15](=[O:21])[CH2:14][CH2:13]4)[CH2:10][CH2:9][C:8]1=[CH:7][C:6](=[O:22])[CH2:5][C@H:4]2[CH3:23]

参加物

実験手順

19-Hydroxy-1β,2β-methylene-4-androstene-3,17-dione, zinc powder, and acetic acid are heated to their reflux temperature for a period of about 1 hour. Upon cooling of the reaction mixture, benzene is added and the resulting suspension filtered. The filtrate is evaporated to dryness under vacuum and the residue remaining is chromatographed on a silica gel column and eluted with methylenechloride. The eluate is evaporated to dryness and the residue is crystallized from an acetone-hexane solution to yield 19-hydroxy-1β-methyl-4-androstene-3,17-dione.