Potassium Sodium Tartrate → HCID 66884704, compound

HRID 1364253Notes

Reaction equation

HRID 1364253 reaction equation
C[O:2][C:3](=O)[CH:4]([CH3:19])[CH2:5][CH2:6][O:7][C:8]1[CH:17]=[C:16]2[C:11]([CH2:12][CH2:13][C:14](=[O:18])[NH:15]2)=[CH:10][CH:9]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[C@H](O)(C([O-])=O)[C@@H](O)C([O-])=O.[Na+].[K+]>O1CCCC1>[OH:2][CH2:3][CH:4]([CH3:19])[CH2:5][CH2:6][O:7][C:8]1[CH:17]=[C:16]2[C:11]([CH2:12][CH2:13][C:14](=[O:18])[NH:15]2)=[CH:10][CH:9]=1

Participants

5

Procedure

6 g of 2-methyl-4-(2-oxo-1,2,3,4-tetrahydroquinolin-7-yloxy)butyric acid methyl ester was added dropwise to a tetrahydrofuran (200 ml) suspension of 1.6 g of lithium aluminum hydride while being stirred under ice-cooling and stirred at the same temperature for 2 hours. While being stirred under ice-cooling, saturated Rochelle salt aqueous solution was added, which was extracted with diethyl ether and, after washed with water, dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (dichloromethane:methanol=40:1), and 2.8 g of 7-(4-hydroxy-3-methylbutoxy)-3,4-dihydro-1H-quinolin-2-one was obtained in the form of a yellow oil.

Workup

  1. temperaturecooling
  2. stirringstirred at the same temperature for 2 hours
  3. stirringWhile being stirred under ice-
  4. temperaturecooling
  5. extractionwhich was extracted with diethyl ether
  6. washafter washed with water
  7. dry with materialdried over magnesium sulfate
  8. customthe solvent was evaporated under reduced pressure
  9. customThe residue was purified by silica gel column chromatography (dichloromethane:methanol=40:1)

Sources & evidence

ORD record
ord-4d2f0f3c166846cfa3152a9da8f659c0
Source dataset
uspto-grants-2011_02
Patent number
US07888362B2

Reaction notes

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