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盐酸 → HCID 90014016,化合物

HRID 1051237
笔记
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反应方程式

HRID 1051237 反应方程式
C([O:3][CH:4](OCC)[CH2:5][N:6]([CH2:9][CH3:10])[CH2:7][CH3:8])C.Cl.[OH:15][S:16]([O-:18])=[O:17].[Na+:19].C(O)C>O>[CH2:7]([N:6]([CH2:9][CH3:10])[CH2:5][CH:4]([OH:3])[S:16]([O-:18])(=[O:17])=[O:15])[CH3:8].[Na+:19]
参与物实验过程后处理来源与证据反应笔记

参与物

6

反应物 4

HCID 313盐酸HCID 702乙醇HCID 77164二乙氨基乙醛缩二乙醇HCID 23665763亚硫酸氢钠

产物 1

HCID 90014016HCID 90014016,化合物

试剂、催化剂与溶剂 1

HCID 962聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]溶剂2 次

实验过程

2,2-diethoxy-N,N-diethylethanamine (140 mg, 0.75 mmol) was added in 0.1 mL H2O. Concentrated HCl (190 mg) was added dropwise in an ice bath. The solution was stirred for 2 hours at 40 degree. NaHSO3 (350 mg, 3.36 mmol) in 0.6 mL H2O was added to the reaction solution in an ice bath and stirred for 1 hour at room temperature, then 0.6 ml ethanol was added and stirred for 1 hour at room temperature. This reaction solution was concentrated, the resulting residue was used directly for the next step.

后处理

  1. stirringstirred for 1 hour at room temperature
  2. stirringstirred for 1 hour at room temperature
  3. concentrationThis reaction solution was concentrated

来源与证据

ORD记录
ord-531037a209a54e8e914edf477127b831
来源数据集
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
专利号
US09388170B2

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