Hydrochloric Acid → Methyl 3-amino-4-(methylamino)benzoate

HRID 23909

反応式

HRID 23909 の反応式
[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[CH:8][C:7]([NH:10][CH3:11])=[C:6]([N+:12]([O-])=O)[CH:5]=1.Cl>[Pd].CO>[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[CH:8][C:7]([NH:10][CH3:11])=[C:6]([NH2:12])[CH:5]=1

参加物

5

反応物 2

HCID 313Hydrochloric AcidHCID 7650848Methyl 4-(methylamino)-3-nitrobenzoate

生成物 1

HCID 15586064Methyl 3-amino-4-(methylamino)benzoate

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

71 g of 4-methylamino-3-nitro-benzoic acid-methyl ester (338 mmol) are hydrogenated in 1.41, of methanol and 67 ml of concentrated aqueous hydrochloric acid in the presence of 15 g of Pd/C (5%) at 2-5 bar, at room temperature. After filtering off the catalysts and distilling off the solvent under vacuum, the residue is dissolved in 200 ml of water, covered with ethyl acetate and basified with a 50% solution of potassium carbonate. The product is extracted in the organic phase, which is again washed with water and then dried over sodium sulphate. After removal of most of the solvent by distillation under vacuum, diethyl ether is added and it is cooled off. The resulting crystals are filtered off. Yield: 54 g (81%); MPt.: 215-220° C. (decomposition).

後処理

  1. filtrationAfter filtering off the catalysts
  2. distillationdistilling off the solvent under vacuum
  3. dissolutionthe residue is dissolved in 200 ml of water
  4. extractionThe product is extracted in the organic phase, which
  5. washis again washed with water
  6. dry with materialdried over sodium sulphate
  7. customAfter removal of most of the solvent
  8. distillationby distillation under vacuum, diethyl ether
  9. additionis added
  10. temperatureit is cooled off
  11. filtrationThe resulting crystals are filtered off

出典と根拠

ORDレコード
ord-eb14e9d5acf3483ebfd7ce658ad744ee
出典データセット
uspto-grants-2005_02
特許番号
US06855713B2

関連ノート

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