Aluminium lithium hydride → HCID 86739149, compound
Reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].C([O:9][C:10](=O)[C@@H:11]([C@@H:26]1[C@:43]2([CH3:44])[C@H:29]([C@H:30]3[C@H:40]([CH2:41][CH2:42]2)[C@:38]2([CH3:39])[C:33]([CH2:34][CH2:35][CH2:36][CH2:37]2)=[CH:32][CH2:31]3)[CH2:28][CH2:27]1)[CH2:12][CH2:13][C:14]([F:25])([F:24])[C:15]([O:18][CH:19]([O:21][CH2:22][CH3:23])[CH3:20])([CH3:17])[CH3:16])C>O1CCCC1.CCOCC>[CH2:22]([O:21][CH:19]([O:18][C:15]([C:14]([F:24])([F:25])[CH2:13][CH2:12][C@H:11]([C@@H:26]1[C@:43]2([CH3:44])[C@H:29]([C@H:30]3[C@H:40]([CH2:41][CH2:42]2)[C@:38]2([CH3:39])[C:33]([CH2:34][CH2:35][CH2:36][CH2:37]2)=[CH:32][CH2:31]3)[CH2:28][CH2:27]1)[CH2:10][OH:9])([CH3:16])[CH3:17])[CH3:20])[CH3:23]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 50 °C
Procedure
To a mixture of 0.20 g (0.0053 mol) of lithium aluminum hydride and 10 mL of tetrahydrofuran at 0° C. was added 2.55 g (0.0034 mol) of [1α,3β]-1,3-bis[tetrahydro-2H-pyran-2-yl)oxy]-25-(1-ethoxyethoxy)-24,24-difluorocholest-5-en-21-oic acid ethyl ester in 35 mL of tetrahydrofuran. The mixture was heated at 50° C. for 1.5 hr, recooled to 0° C., and diluted with 120 mL of ether. The mixture was then quenched with the dropwise addition of 0.40 ml of water and 0.32 mL of 10% aqueous sodium hydroxide. The mixture was stirred at 25° C. for 1 hr and was filtered. The solids were triturated with ether and filtered. Evaporation of solvent afforded [1α,3β]-1,3-bis[tetrahydro-2H-pyran-2-yl)oxy]-25-(1-ethoxyethoxy)-24,24-difluorocholest-5-en-21ol, [α]D20 +4° (c 1, CHCl3).
Workup
- customrecooled to 0° C.
- customThe mixture was then quenched with the dropwise addition of 0.40 ml of water and 0.32 mL of 10% aqueous sodium hydroxide
- filtrationwas filtered
- customThe solids were triturated with ether
- filtrationfiltered
- customEvaporation of solvent
Sources & evidence
- ORD record
- ord-766a03b7daf54fc0a184c5bf10ca5345
- Source dataset
- uspto-grants-1983_12
- Patent number
- US04421690
Reaction notes
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