Hydrochloric Acid → 2-hydroxy-2-phenyl-4-(4-carboxyphenyl)-3(2H)-furanone

HRID 259442Notes

Reaction equation

HRID 259442 reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]([C:15](=[O:24])[C:16]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[O:17])=[CH:11]N(C)C)=[CH:6][CH:5]=1)([OH:3])=[O:2].Cl.[OH-:26].[K+]>>[OH:17][C:16]1([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:15](=[O:24])[C:10]([C:7]2[CH:8]=[CH:9][C:4]([C:1]([OH:3])=[O:2])=[CH:5][CH:6]=2)=[CH:11][O:26]1

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 540610692-(4-Carboxyphenyl)-1-dimethylamino-4-phenyl-1-butene-3,4-dione

Product 1

HCID 203044972-hydroxy-2-phenyl-4-(4-carboxyphenyl)-3(2H)-furanoneYield 71%

Procedure

A solution of 3.23 g of 2-(4-carboxyphenyl)-1-dimethylamino-4-phenyl-1-butene-3,4-dione in 100 ml of 2% potassium hydroxide solution was stirred at room temperature for 5 hrs. The reaction mixture was poured onto 300 ml of ice-water and acidified with 100 ml of 1N hydrochloric acid. The precipitate was collected, washed with water and then dissolved in 300 ml of ether. The solution was dried over anhydrous sodium sulfate. The drying agent was collected and the filtrate was evaporated. Recrystallization from ether gave 2.12 g (71%) of 2-hydroxy-2-phenyl-4-(4-carboxyphenyl)-3(2H)-furanone, m.p. 294°-299° C. dec.

Workup

  1. customThe precipitate was collected
  2. washwashed with water
  3. dissolutiondissolved in 300 ml of ether
  4. dry with materialThe solution was dried over anhydrous sodium sulfate
  5. customThe drying agent was collected
  6. customthe filtrate was evaporated
  7. customRecrystallization from ether

Sources & evidence

ORD record
ord-e7ba624d0a834a649e87796c2fd1ae38
Source dataset
uspto-grants-1977_07
Patent number
US04038289

Reaction notes

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