3beta-Acetoxy-5-pregnene-20-one → HCID 54019415, compound

HRID 362794Notes

Reaction equation

HRID 362794 reaction equation
[BH4-].[Na+].[CH3:3][C:4]([C@@H:6]1[C@@:10]2([CH3:28])[CH2:11][CH2:12][C@@H:13]3[C@@:18]4([CH3:27])[CH2:19][CH2:20][C@H:21]([O:23][C:24]([CH3:26])=[O:25])[CH2:22][C:17]4=[CH:16][CH2:15][C@H:14]3[C@@H:9]2[CH2:8][CH2:7]1)=[O:5]>C(O)C.C(Cl)Cl>[C:24]([O:23][CH:21]1[CH2:20][CH2:19][C@@:18]2([CH3:27])[C:17](=[CH:16][CH2:15][C@@H:14]3[C@@H:13]2[CH2:12][CH2:11][C@@:10]2([CH3:28])[C@H:9]3[CH2:8][CH2:7][C@@H:6]2[CH:4]([OH:5])[CH3:3])[CH2:22]1)(=[O:25])[CH3:26]

Participants

5

Conditions

Temperature
4 °C

Procedure

Sodium borohydride (21 gm) was added to a solution of pregnenolone acetate (100 g, 0.28 mol) in absolute ethanol (1 L) and methylene chloride (0.4 L) at -10° C. After stirring overnight at 4° C., another amount of sodium borohydride (10.5 gm) was added and the reaction stirred at room temperature overnight. The reaction mixture was quenched by pouring into 5% sodium phosphate monobasic (2 L) and extracted with methylene chloride. The organic extracts were dried over anhydrous magnesium sulfate and filtered through a pad of anhydrous sodium sulfate. The solvent was removed by rotoevaporation to give the title compound.

Workup

  1. stirringthe reaction stirred at room temperature overnight
  2. customThe reaction mixture was quenched
  3. additionby pouring into 5% sodium phosphate monobasic (2 L)
  4. extractionextracted with methylene chloride
  5. dry with materialThe organic extracts were dried over anhydrous magnesium sulfate
  6. filtrationfiltered through a pad of anhydrous sodium sulfate
  7. customThe solvent was removed by rotoevaporation

Sources & evidence

ORD record
ord-4baf32291bee48e3a9a76cc40c471ad5
Source dataset
uspto-grants-1999_02
Patent number
US05872126

Reaction notes

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