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Water → 5-(Aminomethyl)-2-chloropyridine

HRID 249470
ノート
印刷プレビュー

反応式

HRID 249470 の反応式
O.NN.[Cl:4][C:5]1[N:10]=[CH:9][C:8]([CH2:11][N:12]2C(=O)C3=CC=CC=C3C2=O)=[CH:7][CH:6]=1.O>CCO>[Cl:4][C:5]1[N:10]=[CH:9][C:8]([CH2:11][NH2:12])=[CH:7][CH:6]=1
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 962WaterHCID 24654Hydrazine hydrate (1:1)HCID 143247132-[(6-Chloropyridin-3-yl)methyl]-1H-isoindole-1,3(2H)-dione

生成物 1

HCID 70209275-(Aminomethyl)-2-chloropyridine収率 70.1%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Hydrazine hydrate (1.7 ml) was added to a refluxing solution of 6.5 g (2.4×10-2 mole) of N-(6-chloro-3-pyridylmethyl)phthalimide in 100 ml of EtOH, and the mixture was further refluxed for 1 hour. After addition of 20 ml of water, the ethanol was distilled off under reduced pressure. Concentrated hydrochloric acid (25 ml) was added to the residue and the mixture was refluxed for 1 hour. After cooling, the reaction mixture was neutralized with NaOH and the aqueous layer was saturated with NaCl and extracted with Et2O. The extract was dried over Na2SO4 and the solvent was distilled off to give 2.4 g of the title compound as a yellow oil.

後処理

  1. temperaturethe mixture was further refluxed for 1 hour
  2. distillationthe ethanol was distilled off under reduced pressure
  3. additionConcentrated hydrochloric acid (25 ml) was added to the residue
  4. temperaturethe mixture was refluxed for 1 hour
  5. temperatureAfter cooling
  6. extractionextracted with Et2O
  7. dry with materialThe extract was dried over Na2SO4
  8. distillationthe solvent was distilled off

出典と根拠

ORDレコード
ord-cee9b61658ec4993a5facdf399428873
出典データセット
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05214152

反応ノート

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