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Hydrazine → HCID 21515433、化合物

HRID 1284329
ノート
印刷プレビュー

反応式

HRID 1284329 の反応式
[Cl:1][C:2]1[N:3]=[N:4][CH:5]=[C:6]([NH2:8])[CH:7]=1.[NH2:9][NH2:10]>>[ClH:1].[ClH:1].[NH2:8][C:6]1[CH:7]=[C:2]([NH:9][NH2:10])[N:3]=[N:4][CH:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 9321HydrazineHCID 140991445-Amino-3-chloro-pyridazine

生成物 1

HCID 21515433HCID 21515433、化合物

実験手順

7 g. of 3-chloro-5-aminopyridazine is added to 125 ml. of hydrazine and the mixture is stirred under nitrogen for 17.5 hours at a temperature below reflux. The reaction mixture is cooled to room temperature, and the residual hydrazine removed by evaporation. The residue is treated with 250 ml. of methanol to extract the product. After separating the extractant and washing the residue with small amounts of methanol, the combined extractant-filtrate is treated with hydrogen chloride gas. The solution is then treated with ether to give a crystalline product which is recrystallized from methanol to give 5-amino-3-hydrazinopyridazine dihydrochloride; m.p. 220°-222°C.

後処理

  1. temperaturebelow reflux
  2. customthe residual hydrazine removed by evaporation
  3. additionThe residue is treated with 250 ml
  4. extractionof methanol to extract the product
  5. customAfter separating the extractant
  6. washwashing the residue with small amounts of methanol
  7. additionthe combined extractant-filtrate is treated with hydrogen chloride gas
  8. additionThe solution is then treated with ether
  9. customto give a crystalline product which
  10. customis recrystallized from methanol

出典と根拠

ORDレコード
ord-e230a57f9374441daf7af5200a81fe3b
出典データセット
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03978057

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート