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Acetic Acid → HCID 10472595, compound

HRID 1607682
Notes
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Reaction equation

HRID 1607682 reaction equation
C(C1[CH:13]=[CH:12][C:6]([NH:7][S:8]([CH3:11])(=[O:10])=[O:9])=[C:5]([O:14][C:15]2[CH:20]=[CH:19][C:18]([F:21])=[CH:17][C:16]=2[F:22])[CH:4]=1)#N.Cl.[C:24]([OH:27])(=[O:26])[CH3:25]>>[F:22][C:16]1[CH:17]=[C:18]([F:21])[CH:19]=[CH:20][C:15]=1[O:14][C:5]1[CH:4]=[C:25]([CH:13]=[CH:12][C:6]=1[NH:7][S:8]([CH3:11])(=[O:9])=[O:10])[C:24]([OH:27])=[O:26]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 176Acetic AcidHCID 313Hydrochloric AcidHCID 10358871N-[4-cyano-2-(2,4-difluorophenoxy)phenyl]methanesulfonamide

Product 1

HCID 10472595HCID 10472595, compound

Procedure

A mixture of 4'-cyano-2'-(2,4-difluorophenoxy)methanesulfonanilide (1.3 g) and concentrated hydrochloric acid (13 ml) in acetic acid (8 ml) was refluxed for 8 hours. The precipitates were filtered, washed with water, dried, and recrystallized from a mixture of ethyl acetate and hexane to give crystals of 3-(2,4-difluorophenoxy)-4-(methanesulfonamido)benzoic acid (0.72 g).

Workup

  1. temperaturewas refluxed for 8 hours
  • filtrationThe precipitates were filtered
  • washwashed with water
  • customdried
  • customrecrystallized from a mixture of ethyl acetate and hexane
  • Sources & evidence

    ORD record
    ord-5dcd9afa03c149bdad9e63bd6b0651e9
    Source dataset
    uspto-grants-1989_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04866091

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes