Water → HCID 19969794, compound

HRID 345837Notes

Reaction equation

HRID 345837 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]=1

Participants

6

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

  1. temperatureunder reflux
  2. filtrationThe salts are filtered off
  3. concentrationthe filtrate is concentrated by evaporation
  4. distillationthe residue is distilled

Sources & evidence

ORD record
ord-c19646dedf9640d49e7dd5d0e6fafd66
Source dataset
uspto-grants-1991_10
Patent number
US05059597

Reaction notes

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