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Methanol → 3-[3-(Naphthalen-1-ylsulfamoyl)-phenyl]-acrylic acid

HRID 2217675
Notes
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Reaction equation

HRID 2217675 reaction equation
C[O:2][C:3](=[O:26])[CH:4]=[CH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([S:12](=[O:25])(=[O:24])[NH:13][C:14]2[C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[CH:17]=[CH:16][CH:15]=2)[CH:7]=1.CO>>[C:14]1([NH:13][S:12]([C:8]2[CH:7]=[C:6]([CH:5]=[CH:4][C:3]([OH:26])=[O:2])[CH:11]=[CH:10][CH:9]=2)(=[O:25])=[O:24])[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]=[CH:16][CH:15]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 887MethanolHCID 670195833-[3-(Naphthalen-1-ylsulfamoyl)-phenyl]-acrylic acid methyl ester

Product 1

HCID 670195673-[3-(Naphthalen-1-ylsulfamoyl)-phenyl]-acrylic acid

Procedure

To a suspension of 3-[3-(naphthalen-1-ylsulfamoyl)phenyl]-acrylic acid methyl ester (14d) (0.29 g, 0.79 mmol) in methanol (3 ml) 1N NaOH solution (2.4 ml, 2.4 mmol) was added and the resultant mixture was stirred at ambient temperature overnight. The reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was acidified with 2N HCl solution and stirred for 30 min. The precipitated solid was filtered, washed with water and dried in desiccator over P2O5. The title compound was obtained as a white solid (0.22 g, 79%).

Workup

  1. additionwas added
  2. customThe reaction mixture was partitioned between ethyl acetate and water
  • filtrationThe precipitated solid was filtered
  • washwashed with water
  • dry with materialdried in desiccator over P2O5
  • Sources & evidence

    ORD record
    ord-c49ce0c4a8c8447b927c4b505d2f3e40
    Source dataset
    uspto-grants-2008_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07407988B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes