Potassium sodium tartarate → 17beta-Acetoxy-17alpha-methyl-3-oxoandrost-4-ene-7alpha-carbonitrile

HRID 2254633Notes

Reaction equation

HRID 2254633 reaction equation
[C:1]([O:4][C@@:5]1([CH3:25])[CH2:10][CH2:9][C@H:8]2[C@H:11]3[C@H:21]([CH2:22][CH2:23][C@:6]12[CH3:7])[C@:19]1([CH3:20])[C:14](=[CH:15][C:16](=[O:24])[CH2:17][CH2:18]1)[CH:13]=[CH:12]3)(=[O:3])[CH3:2].[C-:26]#[N:27].C([Al+]CC)C.C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[K+]>C1(C)C=CC=CC=1.C(OCC)(=O)C>[C:1]([O:4][C@@:5]1([CH3:25])[CH2:10][CH2:9][C@H:8]2[C@H:11]3[C@H:21]([CH2:22][CH2:23][C@:6]12[CH3:7])[C@:19]1([CH3:20])[C:14](=[CH:15][C:16](=[O:24])[CH2:17][CH2:18]1)[CH2:13][C@H:12]3[C:26]#[N:27])(=[O:3])[CH3:2]

Participants

6

Procedure

At room temperature, 17.1 g of 17β-acetoxy-17α-methylandrosta-4,6-dien-3-one [U.S. Pat. No. 3,033,752 (1962)] in 170 ml of toluene is combined with 100 ml of diethyl aluminum cyanide solution (1 mole in toluene). After 24 hours, the reaction mixture is introduced into a potassium sodium tartrate solution, diluted with ethyl acetate, and the mixture is stirred for 1 hour at room temperature, extracted with ethyl acetate, the organic phase is washed with water, dried, and concentrate under vacuum. The resultant crude product is allowed to react in 500 ml of methanol at room temperature with 360 mg of potassium carbonate, the mixture is concentrated under vacuum after 2.5 hours, diluted with ethyl acetate, washed with water, and dried. After the crude product has been chromatographed on silica gel with a methylene chloride (tert-butyl methyl ether) gradient, 13 g of 17β-acetoxy-17α-methyl-3-oxoandrost-4-ene-7α-carbonitrile is obtained, mp 211°-216° C. (from isopropyl ether).

Workup

  1. customAt room temperature
  2. extractionextracted with ethyl acetate
  3. washthe organic phase is washed with water
  4. customdried
  5. concentrationconcentrate under vacuum
  6. customto react in 500 ml of methanol at room temperature with 360 mg of potassium carbonate
  7. concentrationthe mixture is concentrated under vacuum after 2.5 hours
  8. additiondiluted with ethyl acetate
  9. washwashed with water
  10. customdried
  11. customAfter the crude product has been chromatographed on silica gel with a methylene chloride (tert-butyl methyl ether) gradient

Sources & evidence

ORD record
ord-627120541d38480e9ce86b108243e822
Source dataset
uspto-grants-1993_08
Patent number
US05236912

Reaction notes

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