HCID 68807570, compound → HCID 69504664, compound
Reaction equation
[OH:1][C@H:2]1[CH2:24][CH2:23][C@@:22]2([CH3:25])[C:4](=[CH:5][CH2:6][C@@H:7]3[C@@H:21]2[CH2:20][C@@H:19]([OH:26])[C@@:18]2([CH3:27])[C@:8]3([OH:28])[CH2:9][CH2:10][C@@H:11]2[C:12]2(OCCO2)[CH3:13])[CH2:3]1>C(O)(=O)C>[OH:1][C@H:2]1[CH2:24][CH2:23][C@@:22]2([CH3:25])[C:4](=[CH:5][CH2:6][C@@H:7]3[C@@H:21]2[CH2:20][C@@H:19]([OH:26])[C@@:18]2([CH3:27])[C@:8]3([OH:28])[CH2:9][CH2:10][C@@H:11]2[CH2:12][CH3:13])[CH2:3]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The ethylenedioxypregnene (25) (250 mg, 0.64 mmol) is dissolved in acetic acid (13.4 ml) and water which after freeze drying affords the trihydroxy steroid (15) (200 mg, 89%), m.p.: 228°–235° C. (lit. 225°–235° C.), M+348, [αD]20 +35° (lit [αD]20+29°).
Workup
- dry with materialwater which after freeze drying
Sources & evidence
- ORD record
- ord-724f80660c814d04928d93522ddc55a4
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07166611B2
Reaction notes
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