化工社
首页MCP工作台Skills
首页工作台通知我的
llms.txt · MCP 指南隐私政策 · 服务条款 · 支持v1.8.0
  1. 首页
  2. /反应

水合肼 → HCID 178470479,化合物

HRID 44575
笔记
打印预览

反应方程式

HRID 44575 反应方程式
[CH2:1]([O:3][C:4]1[C:5](=O)[CH:6]([C:10](=O)[C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH2:7][CH2:8][CH:9]=1)[CH3:2].O.[NH2:19][NH2:20]>C(O)C>[CH2:1]([O:3][C:4]1[C:5]2[NH:20][N:19]=[C:10]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[C:6]=2[CH2:7][CH2:8][CH:9]=1)[CH3:2]
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 2

HCID 24654水合肼HCID 44235432Ethyl (3-ethoxy-2-oxocyclohex-3-en-1-yl)(oxo)acetate

产物 1

HCID 178470479HCID 178470479,化合物收率 67.7%

试剂、催化剂与溶剂 1

HCID 702乙醇溶剂

实验过程

1.2 g (5 mmol) of ethyl (3-ethoxy-2-oxocyclohex-3-en-1-yl)(oxo)acetate were dissolved in 20 mL of ethanol and 25 mL (5.2 mmol) of hydrazine hydrate 98% were added dropwise. The solution was stirred at room temperature for 5 hours, then heated at 60° C. for further 5 hours. The solvent was removed in vacuo and the residue taken up with diethyl ether and the resulting precipitate collected by filtration giving 0.8 g of the title compound, that was employed in the next step without any further purification.

后处理

  1. temperatureheated at 60° C. for further 5 hours
  2. customThe solvent was removed in vacuo
  3. filtrationthe resulting precipitate collected by filtration

来源与证据

ORD记录
ord-570cf764e18d4fcfa2f471c197fbdb8f
来源数据集
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08541429B2

反应笔记

加载中…

本页导航参与物实验过程后处理来源与证据反应笔记