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Methanesulfonyl chloride → 3-(2,4-Difluorophenylthio)-4-(methanesulfonamido)benzoic acid

HRID 1087212
ノート
印刷プレビュー

反応式

HRID 1087212 の反応式
[NH2:1][C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8]CC)=[O:7])=[CH:4][C:3]=1[S:13][C:14]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][C:15]=1[F:21].[CH3:22][S:23](Cl)(=[O:25])=[O:24]>N1C=CC=CC=1>[F:21][C:15]1[CH:16]=[C:17]([F:20])[CH:18]=[CH:19][C:14]=1[S:13][C:3]1[CH:4]=[C:5]([CH:11]=[CH:12][C:2]=1[NH:1][S:23]([CH3:22])(=[O:25])=[O:24])[C:6]([OH:8])=[O:7]
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 31297Methanesulfonyl chlorideHCID 10040979Ethyl 4-amino-3-(2,4-difluorophenylthio)benzoate

生成物 1

HCID 100439883-(2,4-Difluorophenylthio)-4-(methanesulfonamido)benzoic acid収率 51.6%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

反応条件

温度
60 °C

実験手順

A mixture of ethyl 4-amino-3-(2,4-difluorophenylthio)benzoate (1.1 g) and methanesulfonyl chloride (0.93 g) in pyridine (5 ml) was stirred at 60° C. for 2 hours. The reaction mixture was evaporated. The residue was dissolved in methanol and treated with potassium hydroxide (2 g). The mixture was concentrated and the residue was dissolved in water and washed with chloroform. The aqueous layer was acidified with hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, dried and evaporated. The solid residue was recrystallized from ethanol to give 3-(2,4-difluorophenylthio)-4-(methanesulfonamido)benzoic acid (0.66 g).

後処理

  1. customThe reaction mixture was evaporated
  2. dissolutionThe residue was dissolved in methanol
  3. additiontreated with potassium hydroxide (2 g)
  4. concentrationThe mixture was concentrated
  5. dissolutionthe residue was dissolved in water
  6. washwashed with chloroform
  7. extractionextracted with ethyl acetate
  8. washThe extract was washed with water
  9. customdried
  10. customevaporated
  11. customThe solid residue was recrystallized from ethanol

出典と根拠

ORDレコード
ord-fd53285f608047cd85045982a19482a6
出典データセット
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05034417

反応ノート

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