3beta-Acetoxy-5-pregnene-20-one → HCID 54019415, compound
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
Reactant 2
Product 1
Reagents, catalysts & solvents 2
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
- stirringthe reaction stirred at room temperature overnight
- customThe reaction mixture was quenched
- additionby pouring into 5% sodium phosphate monobasic (2 L)
- extractionextracted with methylene chloride
- dry with materialThe organic extracts were dried over anhydrous magnesium sulfate
- filtrationfiltered through a pad of anhydrous sodium sulfate
- 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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