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ethyl P-methyl-2-nitro-5-chlorophenylphosphinate → ethyl P-methyl-2-amino-5-chlorophenylphosphinate

HRID 463561
笔记
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反应方程式

HRID 463561 反应方程式
[CH3:1][P:2]([C:7]1[CH:12]=[C:11]([Cl:13])[CH:10]=[CH:9][C:8]=1[N+:14]([O-])=O)(=[O:6])[O:3][CH2:4][CH3:5]>CO.[Pd]>[CH3:1][P:2]([C:7]1[CH:12]=[C:11]([Cl:13])[CH:10]=[CH:9][C:8]=1[NH2:14])(=[O:6])[O:3][CH2:4][CH3:5]
参与物实验过程后处理来源与证据反应笔记

参与物

4

反应物 1

HCID 53860251ethyl P-methyl-2-nitro-5-chlorophenylphosphinate

产物 1

HCID 53901381ethyl P-methyl-2-amino-5-chlorophenylphosphinate

试剂、催化剂与溶剂 2

HCID 23938钯碳催化剂HCID 887Methanol溶剂

实验过程

Ethyl P-methyl-2-nitro-5-chlorophenylphosphinate (1.7 g, 7.5 mmol) dissolved in methanol (25 ml) is added to 200 mg of 5% palladium on carbon. The mixture is hydrogenated at 32 psi for 1 hour. The catalyst is then filtered off and the filtrate is evaporated to dryness to give ethyl P-methyl-2-amino-5-chlorophenylphosphinate.

后处理

  1. filtrationThe catalyst is then filtered off
  2. customthe filtrate is evaporated to dryness

来源与证据

ORD记录
ord-0f90b9e8e3224c6c9f66c15bc4a19f4a
来源数据集
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
专利号
US04520197

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记