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Formic Acid → 2-Fluoro-4-sulfamoylbenzoic acid

HRID 1992094
ノート
印刷プレビュー

反応式

HRID 1992094 の反応式
[F:1][C:2]1[CH:3]=[C:4]([S:9]([NH2:12])(=[O:11])=[O:10])[CH:5]=[CH:6][C:7]=1C.[C:13](=[O:16])([O-])[O-:14].[Na+].[Na+].[Mn]([O-])(=O)(=O)=O.[K+].C(O)=O>O>[NH2:12][S:9]([C:4]1[CH:5]=[CH:6][C:7]([C:13]([OH:14])=[O:16])=[C:2]([F:1])[CH:3]=1)(=[O:11])=[O:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 284Formic AcidHCID 10340Sodium CarbonateHCID 516875Potassium PermanganateHCID 20641383-Fluoro-4-methylbenzenesulfonamide

生成物 1

HCID 591287362-Fluoro-4-sulfamoylbenzoic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a stirred solution of 3-fluoro-4-methyl-benzenesulfonamide (prepared above) in 50 mL of water was added sodium carbonate (0.53 g, 5 mmol) and potassium permanganate (3.16 g, 20 mmol) portionwise over three hours at 50˜60° C. The resulting mixture was stirred for further 8 hours at this temperature before 0.2 mL of formic acid was added to quench the excess of potassium permanganate. The mixture was then filtered through celite while it was still hot and further washed with the hot water. The filtrate was concentrated to ˜30 mL and adjusted to pH 9˜10. The filtration was applied again to remove non-oxidized starting material. The final filtrate was acidified with HCl (conc.) to ˜pH 1 and 4-(aminosulfonyl)-2-fluorobenzoic acid was precipitated and collected by filtration as white solid (1.10 g, 50%).

後処理

  1. additionwas added
  2. customto quench the excess of potassium permanganate
  3. filtrationThe mixture was then filtered through celite while it
  4. washfurther washed with the hot water
  5. concentrationThe filtrate was concentrated to ˜30 mL
  6. filtrationThe filtration
  7. customto remove non-oxidized
  8. customwas precipitated
  9. filtrationcollected by filtration as white solid (1.10 g, 50%)

出典と根拠

ORDレコード
ord-8e653d35cea14be2b08c99ef74ca0a62
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07645771B2

反応ノート

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