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

HRID 1820824
ノート
印刷プレビュー

反応式

HRID 1820824 の反応式
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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
60 °C

実験手順

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%)

後処理

  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

出典と根拠

ORDレコード
ord-2d6e8cf689d9442f8258a94f91e35e10
出典データセット
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07605163B2

反応ノート

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