Hydrochloric Acid → 13beta-Propyl-17beta-hydroxy-gon-4-en-3-one

HRID 1077184ノート

反応式

HRID 1077184 の反応式
Cl.[CH2:2]([C@:5]12[CH2:13][CH2:12][C@@H:11]3[C:14]4[CH2:15][CH:16]=[C:17]([O:22]C)[CH2:18][C:19]=4[CH2:20][CH2:21][C@H:10]3[C@@H:9]1[CH2:8][CH2:7][C@@H:6]2[OH:24])[CH2:3][CH3:4].CO>O>[CH2:2]([C@:5]12[CH2:13][CH2:12][C@@H:11]3[C@@H:14]4[C:19]([CH2:20][CH2:21][C@H:10]3[C@@H:9]1[CH2:8][CH2:7][C@@H:6]2[OH:24])=[CH:18][C:17](=[O:22])[CH2:16][CH2:15]4)[CH2:3][CH3:4]

参加物

5

実験手順

Add 3N hydrochloric acid (1 cc.) to a solution of 13β-n-propyl-3-methoxy-gona-2,5(10)-dien-17β-ol (0.61 g.) in boiling methanol (70 cc.) and cool the mixture immediately and allow to stand for 41/2 hours. Pour the product into water (300 cc.) and extract the mixture with ether; work up in the usual way to give as residue an amorphous solid (0.6 g.). Crystallize this solid from a mixture of ether and hexane. Take up the resulting solid in benzene (20 cc.) and chromatograph on a column of neutral alumina. Elute the product with ether and recrystallize from a mixture of ether and hexane to obtain 13β-n-propyl-17β-hydroxy-gon-4-en-3-one (0.08 g.), mp. 126°-7°; ultraviolet absorption peak at 240 mμ (ε15,000); infrared absorption peaks at 2.92, 6.01, 6.20 μ. Evaporation of the mother liquors gives a second, polymorphic, form of the same substance (0.17 g.), m.p. 144°-5° , having ultraviolet and infrared spectra identical with the first material; a mixture of the two forms has m.p. 144°-5°.

後処理

  1. temperaturecool the mixture immediately
  2. custom2 hours
  3. extractionextract the mixture with ether
  4. customwork up in the usual way to give as residue an amorphous solid (0.6 g.)
  5. customCrystallize this solid
  6. additionfrom a mixture of ether and hexane
  7. washElute the product with ether
  8. customrecrystallize from a mixture of ether and hexane

出典と根拠

ORDレコード
ord-ba8e9e360d0a4bc8b505d223ae501de5
出典データセット
uspto-grants-1976_05
特許番号
US03959322

反応ノート

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