Water → HCID 19969794, compound
Reaction equation
[CH2:1]([N:8]=[C:9]([CH:11]1[CH:16]([C:17](O)=O)[CH2:15][CH:14]([CH3:20])[CH2:13][NH:12]1)O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[CH2:1]([N:8]1[CH2:9][CH:11]2[CH:16]([CH2:15][CH:14]([CH3:20])[CH2:13][NH:12]2)[CH2:17]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
13.0 g of crude 5-methyl-hexahydropyridine-2,3-dicarboxylic acid N-benzylimide are added in the form of a solution in 50 ml of absolute tetrahydrofuran to 4.6 g (0.12 mol) of lithium aluminum hydride in 100 ml of absolute tetrahydrofuran, already present in the vessel. Then the mixture is boiled for 17 hours under reflux. 4.6 g of water in 14 ml of tetrahydrofuran, 4.6 g of 10% strength sodium hydroxide solution and 13.8 g of water are added dropwise one after the other. The salts are filtered off, the filtrate is concentrated by evaporation and the residue is distilled.
Workup
- temperatureunder reflux
- filtrationThe salts are filtered off
- concentrationthe filtrate is concentrated by evaporation
- distillationthe residue is distilled
Sources & evidence
- ORD record
- ord-300848654474409daf1bf1ebfca5de6a
- Source dataset
- uspto-grants-1997_03
- Patent number
- US05607942
Reaction notes
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