Sodium Hydroxide → HCID 12897040, compound

HRID 1980902Notes

Reaction equation

HRID 1980902 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([Cl:9])=[CH:4][C:3]=1[S:10][C:11]1[NH:15][CH:14]=[C:13]([C:16]([O:18]C)=[O:17])[CH:12]=1.[OH-].[Na+]>CO>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([Cl:9])=[CH:4][C:3]=1[S:10][C:11]1[NH:15][CH:14]=[C:13]([C:16]([OH:18])=[O:17])[CH:12]=1

Participants

4

Reactant 2

HCID 14798Sodium Hydroxide2×HCID 12897049HCID 12897049, compound

Product 1

HCID 12897040HCID 12897040, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent2×

Procedure

Methyl 5-(2,4,5-trichlorophenylthio)pyrrole-3-carboxylate (2.1 g.) was combined with 20 ml. of methanol and 20 ml. of 1N sodium hydroxide and heated to reflux. Additional 1N sodium hydroxide was added in an amount sufficient to obtain a solution. Reflux was continued for 2.5 hours, the methanol was then allowed to evaporate, and the aqueous residue was diluted with approximately one volume of water and extracted twice with ether. The aqueous phase was cooled in an ice-water bath and acidified with conc. hydrochloric acid. Crude product (1.65 g., m.p. 210°-215° C.) was recovered by filtration. Recrystallization from methanol/water afforded purified 5-(2,4,5-trichlorophenylthio)pyrrole-3-carboxylic acid (1.01 g., m.p. 215°-217° C.).

Workup

  1. customto obtain a solution
  2. temperatureReflux
  3. customto evaporate
  4. additionthe aqueous residue was diluted with approximately one volume of water
  5. extractionextracted twice with ether
  6. temperatureThe aqueous phase was cooled in an ice-water bath
  7. filtrationCrude product (1.65 g., m.p. 210°-215° C.) was recovered by filtration
  8. customRecrystallization from methanol/water
  9. customafforded
  10. custompurified 5-(2,4,5-trichlorophenylthio)pyrrole-3-carboxylic acid (1.01 g., m.p. 215°-217° C.)

Sources & evidence

ORD record
ord-d511595488a5443198e5b5d664f2c8ca
Source dataset
uspto-grants-1985_04
Patent number
US04511575

Reaction notes

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