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Ammonium Chloride → 4-amino-2-fluoro-N-methoxy-N-methylbenzamide

HRID 13419
ノート
印刷プレビュー

反応式

HRID 13419 の反応式
[Cl-].[NH4+:2].[F:3][C:4]1[CH:15]=[CH:14][CH:13]=[CH:12][C:5]=1[C:6]([N:8]([O:10][CH3:11])[CH3:9])=[O:7]>CO.O.[Fe]>[NH2:2][C:14]1[CH:13]=[CH:12][C:5]([C:6]([N:8]([O:10][CH3:11])[CH3:9])=[O:7])=[C:4]([F:3])[CH:15]=1
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 2

HCID 25517Ammonium ChlorideHCID 183575562-fluoro-N-methoxy-N-methylbenzamide

生成物 1

HCID 231456994-amino-2-fluoro-N-methoxy-N-methylbenzamide

試薬・触媒・溶媒 3

HCID 23925Iron触媒HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

15.2 g of ammonium chloride and 8 g of iron powder were added to a suspension of 10.84 g of 2-fluoro-N-methoxy-N-methylbenzamide in 60 ml of methanol and 30 ml of water, and the reaction liquid was heated under reflux for 3 hours. The reaction liquid was filtered through Celite, and the solvent was evaporated away under reduced pressure. The resulting residue was diluted with ethyl acetate, washed with water, and dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=9/1 to 1/2 to obtain the entitled compound as a brown oily substance.

後処理

  1. customthe reaction liquid
  2. temperaturewas heated
  3. temperatureunder reflux for 3 hours
  4. customThe reaction liquid
  5. filtrationwas filtered through Celite
  6. customthe solvent was evaporated away under reduced pressure
  7. additionThe resulting residue was diluted with ethyl acetate
  8. washwashed with water
  9. dry with materialdried with anhydrous magnesium sulfate
  10. customThe solvent was evaporated away under reduced pressure
  11. customthe resulting residue was purified through silica gel column chromatography (
  12. customhexane/ethyl acetate=9/1 to 1/2 to obtain the entitled compound as a brown oily substance

出典と根拠

ORDレコード
ord-5f7d2768bf7e4062b30e215939d2ca76
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07728025B2

反応ノート

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