Sodium Hydroxide → HCID 178524718, compound

HRID 2305466Notes

Reaction equation

HRID 2305466 reaction equation
[OH:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([C:12]([F:15])([F:14])[F:13])=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[C:16]([O:18]CC)=[O:17].[OH-].[Na+]>CO>[OH:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([C:12]([F:15])([F:13])[F:14])=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[C:16]([OH:18])=[O:17]

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 178469560HCID 178469560, compound

Product 1

HCID 178524718HCID 178524718, compoundYield 28.7%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A mixture of ethyl 4-hydroxy-7-(trifluoromethyl)-3-quinolinecarboxylate (43.4 g, 0.521 mol) and 10% sodium hydroxide (150 mL) was heated to reflux. Most of the ester did not dissolve so methanol (150 mL) was added over the course of an hour to facilitate dissolution. After refluxing for 2 hours a solution was obtained. The solution was refluxed for an additional 2 hours and then allowed to cool to ambient temperature overnight. The methanol was removed under reduced pressure and the resulting aqueous solution was acidified with concentrated hydrochloric acid. The resulting precipitate was isolated by filtration, washed with water and then dried in a vacuum oven at 120° C. for 24 hours to provide 38.5 g of 4-hydroxy-7-(trifluoromethyl)-3-quinolinecarboxylic acid as a white solid.

Workup

  1. temperaturewas heated to reflux
  2. additionwas added over the course of an hour
  3. dissolutiondissolution
  4. temperatureAfter refluxing for 2 hours a solution
  5. customwas obtained
  6. temperatureThe solution was refluxed for an additional 2 hours
  7. customThe methanol was removed under reduced pressure
  8. customThe resulting precipitate was isolated by filtration
  9. washwashed with water
  10. customdried in a vacuum oven at 120° C. for 24 hours

Sources & evidence

ORD record
ord-b02c7c239fa94952aac9c0864a8de07f
Source dataset
uspto-grants-2002_08
Patent number
US06440992B1

Reaction notes

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