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

HRID 434511

Reaction equation

HRID 434511 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-b31b37c0d51d44f59c5415282e5f735b
Source dataset
uspto-grants-1983_08
Patent number
US04397847

Linked notes

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