Monobasic potassium phosphate → 5,8-Dihydroquinoline-5,8-dione

HRID 2308947Notes

Reaction equation

HRID 2308947 reaction equation
[OH:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2.P([O-])(O)(O)=[O:13].[K+].N(S([O-])(=O)=O)(S([O-])(=O)=O)[O].[K+].[K+]>CO.O>[N:7]1[C:8]2[C:9](=[O:13])[CH:10]=[CH:11][C:2](=[O:1])[C:3]=2[CH:4]=[CH:5][CH:6]=1

Participants

6

Reactant 3

HCID 516951Monobasic potassium phosphateHCID 3032624Potassium nitrosodisulfonateHCID 135441757Quinolin-5-ol

Product 1

HCID 3883065,8-Dihydroquinoline-5,8-dioneYield 47.2%

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 962WaterSolvent

Procedure

To a solution of 23.2 g of 5-hydroxyquinoline in 1600 ml of methanol in an ice bath was added a total of 36 g of potassium dihydrogen phosphate and 96 g of potassium nitroso disulfonate in 8.8 liters of water in five portions over a 1 hour period. The mixture was then stirred overnight at room temperature, followed by extraction with four 1500 ml portions of chloroform. The extracts were combined, dried, filtered through alumina and evaporated to dryness, giving 12.0 g of crude product. An analytical sample was prepared by crystallization from petroleum ether, mp 110° C.

Workup

  1. extractionfollowed by extraction with four 1500 ml portions of chloroform
  2. customdried
  3. filtrationfiltered through alumina
  4. customevaporated to dryness

Sources & evidence

ORD record
ord-ad7559ae3c4144d18cc6537b4e9b745b
Source dataset
uspto-grants-1987_09
Patent number
US04692449

Reaction notes

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