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Formic Acid → 2-Nitrobenzene-1,3-diamine

HRID 981813
ノート
印刷プレビュー

反応式

HRID 981813 の反応式
Cl[C:2]1[CH:7]=[C:6]([NH2:8])[C:5]([N+:9]([O-:11])=[O:10])=[C:4]([NH2:12])[CH:3]=1.C(O)=O>C(N(CC)CC)C.[Pd]>[NH2:8][C:6]1[CH:7]=[CH:2][CH:3]=[C:4]([NH2:12])[C:5]=1[N+:9]([O-:11])=[O:10]
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

5

反応物 2

HCID 284Formic AcidHCID 20071078HCID 20071078、化合物

生成物 1

HCID 141474902-Nitrobenzene-1,3-diamine

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 8471Triethylamine溶媒

反応条件

温度
90 °C

実験手順

68 mg of palladium at a concentration of 10% on charcoal are added to 0.016 mole (3 g) of 4-chloro-2,6-diaminonitro-benzene in 6 ml of triethylamine, and 1.32 ml of formic acid are then added dropwise. A high exothermicity is noted. The reaction medium is heated to 90° C. for 1 hour 30. After dilution of the reaction mixture with ethanol, the catalyst is removed by hot filtration. The filtrate, evaporated to dryness under reduced pressure, enables a dry extract to be obtained. After dilution of the dry extract with water, the expected product precipitates. After filtration and washing with water, followed by drying under vacuum in the presence of phosphorus pentoxide, it is recrystallized from toluene. It melts at 142° C. (literature 141° C., 145° C.).

後処理

  1. additionare then added dropwise
  2. customAfter dilution of the reaction mixture with ethanol, the catalyst is removed by hot filtration
  3. customThe filtrate, evaporated to dryness under reduced pressure
  4. extractionextract
  5. customto be obtained
  6. extractionAfter dilution of the dry extract with water
  7. customthe expected product precipitates
  8. filtrationAfter filtration
  9. washwashing with water
  10. dry with materialby drying under vacuum in the presence of phosphorus pentoxide, it
  11. customis recrystallized from toluene
  12. customIt melts at 142° C. (literature 141° C., 145° C.)

出典と根拠

ORDレコード
ord-2d58795f0f45483ab6f6697622e6a4c0
出典データセット
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04992586

反応ノート

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