Water → HCID 68807570, 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]43[O:28][CH:9]4[CH2:10][C@@H:11]2[C:12]2([O:17][CH2:16][CH2:15][O:14]2)[CH3:13])[CH2:3]1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[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([O:17][CH2:16][CH2:15][O:14]2)[CH3:13])[CH2:3]1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
The 14,15-epoxide (24) (300 mg, 0,77 mmol) in dry tetrahydrofuran (10 ml) is added to a suspension of lithium aluminium hydride (300 mg, 7,89 mmol) in tetrahydrofuran and the reaction refluxed for 48 h. After the addition of water (0,3 ml), sodium hydroxide (15% soln, 0,3 ml) and filtration as described earlier, the mixture is purified by silica gel column chromatography using methanol: chloroform (1:9) as solvent to give the trihydroxy pregnene (25) (250 mg, 83%).
Workup
- temperaturethe reaction refluxed for 48 h
- filtration0,3 ml) and filtration
- customthe mixture is purified by silica gel column chromatography
Sources & evidence
- ORD record
- ord-1dbf7ee086c9401d9aa4489a60b4d71d
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06376657B1
Reaction notes
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