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Methanol → 3-(3-p-Tolylsulfamoyl-phenyl)-acrylic acid

HRID 351035
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인쇄 미리보기

반응식

HRID 351035 반응식
C[O:2][C:3](=[O:23])[CH:4]=[CH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([S:12](=[O:22])(=[O:21])[NH:13][C:14]2[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][CH:15]=2)[CH:7]=1.CO>>[C:17]1([CH3:20])[CH:16]=[CH:15][C:14]([NH:13][S:12]([C:8]2[CH:7]=[C:6]([CH:5]=[CH:4][C:3]([OH:23])=[O:2])[CH:11]=[CH:10][CH:9]=2)(=[O:21])=[O:22])=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 887MethanolHCID 670195113-(3-p-Tolylsulfamoyl-phenyl)-acrylic acid methyl ester

생성물 1

HCID 670195353-(3-p-Tolylsulfamoyl-phenyl)-acrylic acid수율 87.5%

실험 절차

To a suspension of 3-(3-p-tolylsulfamoyl-phenyl)-acrylic acid methyl ester (4d) (0.89 g, 2.70 mmol) in methanol (12 ml) 1N NaOH solution (8.10 ml, 8.10 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 to give the title compound as a white solid (0.75 g, 87%).

후처리

  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
  • 출처 및 근거

    ORD 기록
    ord-3343742bb66743bdb2ee7ae0517581aa
    출처 데이터셋
    uspto-grants-2007_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07183298B2

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