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
5
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
- additionTo this solution was added dropwise
- stirringThe mixture was then stirred at ambient temperature
- filtrationfiltered
- customto remove the triethylamine hydrochloride
- additionafter the addition of 50 ml of anhydrous diethylether
- customThe filtrates were stripped on a rotary evaporator
- customto yield a red-brown oil which
- distillationwas distilled under high vacuum
- 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
- 特許番号
- US04203932
関連ノート
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