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Acetyl chloride → 1-Acetyl-2-Diethoxyphosphoryl Hydrazine

HRID 1395391
ノート
印刷プレビュー

反応式

HRID 1395391 の反応式
[CH2:1]([O:3][P:4]([NH:9][NH2:10])(=[O:8])[O:5][CH2:6][CH3:7])[CH3:2].C(N(CC)CC)C.[C:18](Cl)(=[O:20])[CH3:19]>ClCCl>[C:18]([NH:10][NH:9][P:4]([O:5][CH2:6][CH3:7])([O:3][CH2:1][CH3:2])=[O:8])(=[O:20])[CH3:19]
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 6367Acetyl chlorideHCID 8471TriethylamineHCID 143340Phosphorohydrazidic acid, diethyl ester

生成物 1

HCID 125485571-Acetyl-2-Diethoxyphosphoryl Hydrazine

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

Diethylphosphorohydrazidate (5.3 g) and triethylamine (13 ml) were dissolved in dichloromethane (15 ml). To this solution was added dropwise with stirring and cooling a solution of acetyl chloride (7.4 g) in dichloromethane (15 ml). The mixture was then stirred at ambient temperature and then filtered to remove the triethylamine hydrochloride after the addition of 50 ml of anhydrous diethylether. The filtrates were stripped on a rotary evaporator to yield a red-brown oil which was distilled under high vacuum to give a pale yellow liquid, b.p. 180° C./1 mm, identified as the product.

後処理

  1. additionTo this solution was added dropwise
  2. stirringThe mixture was then stirred at ambient temperature
  3. filtrationfiltered
  4. customto remove the triethylamine hydrochloride
  5. additionafter the addition of 50 ml of anhydrous diethylether
  6. customThe filtrates were stripped on a rotary evaporator
  7. customto yield a red-brown oil which
  8. distillationwas distilled under high vacuum
  9. customto give a pale yellow liquid, b.p. 180° C./1 mm

出典と根拠

ORDレコード
ord-e7333ed741b948dc9645cae461eecfb7
出典データセット
uspto-grants-1980_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04203932

反応ノート

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