HCID 11195250, compound → HCID 20453110, compound
Reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].C([O:9][C:10](=O)[CH2:11][C:12]([CH:15]1[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1)([OH:14])[CH3:13])C>CCOCC>[CH:15]1([C:12]([OH:14])([CH3:13])[CH2:11][CH2:10][OH:9])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a slurry of lithium aluminium hydride (6.39 g, 0.168 mol) in ether (250 ml), in an atmosphere of nitrogen and cooled in an ice-bath was added dropwise ethyl-3-cyclohexyl-3-hydroxy-butyrate (36 g, 0.168 mol) in ether (100 ml). After complete addition of the ester the resultant mixture was boiled at reflux for 1 hr, then cooled in an ice-bath. Excess lithium aluminium hydride was destroyed by successive dropwise addition of water (7 ml), 10% sodium hydroxide solution (7 ml) and water (21 ml). The reaction mixture was filtered, the filter cake washed with ether (2×100 ml) and the filtrate washed with saturated sodium chloride solution (1×250 ml) and then dried (Na2SO4). This mixture was filtered and the filtrate evaporated in vacuo to remove ether to give 3-cyclohexylbutane-1,3-diol (25 g) as an oil.
Workup
- temperatureat reflux for 1 hr
- temperaturecooled in an ice-bath
- customExcess lithium aluminium hydride was destroyed by successive dropwise addition of water (7 ml), 10% sodium hydroxide solution (7 ml) and water (21 ml)
- filtrationThe reaction mixture was filtered
- washthe filter cake washed with ether (2×100 ml)
- washthe filtrate washed with saturated sodium chloride solution (1×250 ml)
- dry with materialdried (Na2SO4)
- filtrationThis mixture was filtered
- customthe filtrate evaporated in vacuo
- customto remove ether
Sources & evidence
- ORD record
- ord-5703cc9aff024f389ba4a9974678d246
- Source dataset
- uspto-grants-1984_07
- Patent number
- US04460595
Reaction notes
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