Tetrahydrofuran → [1alpha,3beta]-1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]androst-5-en-17-one

HRID 745641

Reaction equation

HRID 745641 reaction equation
[OH: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@@H:4]([OH:22])[CH2:3]1.[O:23]1[CH2:27][CH2:26][CH2:25][CH2:24]1.[O:28]1[CH:33]=[CH:32][CH2:31][CH2:30][CH2:29]1.O.[C:35]1(C)C=CC(S(O)(=O)=O)=CC=1>C(Cl)Cl>[O:23]1[CH2:27][CH2:26][CH2:25][CH2:24][CH:35]1[O: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@@H:4]([O:22][CH:33]2[CH2:32][CH2:31][CH2:30][CH2:29][O:28]2)[CH2:3]1

Participants

6

Procedure

A mixture of 0.91 g (0.0030 mol) of 1α,3β-dihydroxyandrost-5-en-17-one [R. M. Dodson, A. H. Goldkamp and R. D. Muir, J.Amer.Chem.Soc., 82, 4026 (1960)], 15 mL of tetrahydrofuran, 1.26 g (0.015 mol) of 3,4-dihydro-2H-pyran and 0.028 g of p-toluenesulfonic acid monohydrate was stirred at 25° for 18 hr. The mixture was diluted with methylene chloride. This solution was then washed with saturated aqueous sodium bicarbonate solution. The organic phase was dried over anhydrous magnesium sulfate, filtered and evaporated to dryness to yield oily [1α,3β]-1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]androst-5-en-17-one, [α]D20 +34.3° (c 1, CHCl3).

Workup

  1. washThis solution was then washed with saturated aqueous sodium bicarbonate solution
  2. dry with materialThe organic phase was dried over anhydrous magnesium sulfate
  3. filtrationfiltered
  4. customevaporated to dryness

Sources & evidence

ORD record
ord-57c4f52724f54c2388446475f8e525ab
Source dataset
uspto-grants-1986_07
Patent number
US04599330

Linked notes

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