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Methanol → Methyl 3-aminocinnamate

HRID 400088
ノート
印刷プレビュー

反応式

HRID 400088 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]([CH:12]=[CH:13][CH:14]=1)[CH:7]=[CH:8][C:9]([OH:11])=[O:10])([O-])=O.[CH3:15]O.S(=O)(=O)(O)O>O>[NH2:1][C:4]1[CH:5]=[C:6]([CH:12]=[CH:13][CH:14]=1)[CH:7]=[CH:8][C:9]([O:11][CH3:15])=[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

5

反応物 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 683902-Propenoic acid, 3-(3-nitrophenyl)-

生成物 1

HCID 54385173Methyl 3-aminocinnamate

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

While mixing and stirring 193 g of 3-nitrocinnamic acid, 2 of methanol and 50 g of concentrated sulfuric acid, the mixture was heated under reflux for 2 hours. The reaction solution was poured into water and the crystals obtained were filtered. To a reaction solution under heat-refluxing while mixing and stirring 2 of 2-propanol, 200 ml of water, 20 g of ammonium chloride and 200 g of reduced iron, the crystals obtained above were gradually added, and the solution was further heated under reflux for one hour. The reaction solution still being hot was filtered, the filtrate was poured into 10 of water, and the crystals (methyl 3-aminocinnamate) obtained were collected by filtration. Yield: 108 g.

後処理

  1. additionWhile mixing
  2. temperaturethe mixture was heated
  3. temperatureunder reflux for 2 hours
  4. customthe crystals obtained
  5. filtrationwere filtered
  6. temperatureTo a reaction solution under heat-refluxing
  7. additionwhile mixing
  8. customthe crystals obtained
  9. additionabove were gradually added
  10. temperaturethe solution was further heated
  11. temperatureunder reflux for one hour
  12. filtrationThe reaction solution still being hot was filtered
  13. additionthe filtrate was poured into 10 of water

出典と根拠

ORDレコード
ord-8c73c921353749408d75b936532bd28c
出典データセット
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05827638

反応ノート

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