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Sodium Hydroxide → 2-(4-Methoxy-benzyloxy)-5-sulfamoyl-benzoic acid

HRID 2251279
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인쇄 미리보기

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HRID 2251279 반응식
C[O:2][C:3](=[O:24])[C:4]1[CH:9]=[C:8]([S:10](=[O:13])(=[O:12])[NH2:11])[CH:7]=[CH:6][C:5]=1[O:14][CH2:15][C:16]1[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[CH:18][CH:17]=1.[OH-].[Na+]>C1COCC1>[CH3:23][O:22][C:19]1[CH:18]=[CH:17][C:16]([CH2:15][O:14][C:5]2[CH:6]=[CH:7][C:8]([S:10](=[O:13])(=[O:12])[NH2:11])=[CH:9][C:4]=2[C:3]([OH:24])=[O:2])=[CH:21][CH:20]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 690375322-(4-Methoxy-benzyloxy)-5-sulfamoyl-benzoic acid methyl ester

생성물 1

HCID 690382462-(4-Methoxy-benzyloxy)-5-sulfamoyl-benzoic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
60 °C

실험 절차

To 2.5 mmol 2-(4-methoxy-benzyloxy)-5-sulfamoyl-benzoic acid methyl ester in 6 ml THF was added 5 mmol 2 M aq NaOH, and the mixture was heated at 60° C. for 30 min. The mixture was then cooled to RT and extracted twice with ethyl acetate. The aqueous phase was acidified to pH 1 with 5 M aq HCl and extracted with ethyl acetate. The combined organic phases were washed with saturated aq NaCl and dried with Na2SO4. Evaporation in vacuo afforded the title compound. MS (m/e): 336.1 ([M−H]−, 100%)

후처리

  1. temperatureThe mixture was then cooled to RT
  2. extractionextracted twice with ethyl acetate
  3. extractionextracted with ethyl acetate
  4. washThe combined organic phases were washed with saturated aq NaCl
  5. dry with materialdried with Na2SO4
  6. customEvaporation in vacuo

출처 및 근거

ORD 기록
ord-d1ba224c654540969b4691b291c59317
출처 데이터셋
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07319099B2

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