Acetic Acid → HCID 70459693, compound
Reaction equation
C(O)(=O)C.Cl[CH2:6][C:7](=[O:30])[C@@:8]1([OH:29])[C@:25]2([CH3:26])[C@H:11]([C@H:12]3[C@H:22]([CH2:23][CH2:24]2)[C@:20]2([CH3:21])[C:15](=[CH:16][C:17](=[O:27])[CH2:18][CH2:19]2)[CH2:14][CH2:13]3)[CH2:10][C:9]1=[CH2:28]>C(OCC)(=O)C.[Zn]>[OH:29][C@@:8]1([C@:25]2([CH3:26])[C@H:11]([C@H:12]3[C@H:22]([CH2:23][CH2:24]2)[C@:20]2([CH3:21])[C:15](=[CH:16][C:17](=[O:27])[CH2:18][CH2:19]2)[CH2:14][CH2:13]3)[CH2:10][C:9]1=[CH2:28])[C:7](=[O:30])[CH3:6]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Zinc dust (0.030 mg) and glacial acetic acid (0.13 ml) is added to a solution of 21-chloro-17β-hydroxy-16-methylenepregn-4-ene-3,20-dione (III, EXAMPLE 40B, 0.050 g) in ethyl acetate (1.5 ml). The reaction system is purged with nitrogen and warmed to 45°. After stirring for 16.5 hr, THF (5 ml) is added and the mixture is filtered thru celite to remove the remaining zinc. The filtrate is then partitioned between water (5 ml) and ether (5 ml). The organic extract is washed with sodium bicarbonate (5%) and water, dried over sodium sulfate and concentrated to give the title compound, NMR (CD2Cl2) 0.87, 1.17, 2.20, 3.40, 5.10 and 5.65 δ.
Workup
- customThe reaction system is purged with nitrogen
- temperaturewarmed to 45°
- additionTHF (5 ml) is added
- filtrationthe mixture is filtered thru celite
- customto remove the remaining zinc
- customThe filtrate is then partitioned between water (5 ml) and ether (5 ml)
- extractionThe organic extract
- washis washed with sodium bicarbonate (5%) and water
- dry with materialdried over sodium sulfate
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-5bbd0dd9bfb948d7a9b441ee53d34d86
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04921638
Reaction notes
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