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异氰酸甲酯 → 2,6-Diethyl-2,3,6-trimethyl-4-piperidyl methylcarbamate

HRID 1391237
笔记
打印预览

反应方程式

HRID 1391237 反应方程式
[CH2:1]([C:3]1([CH3:14])[CH:8]([CH3:9])[CH:7]([OH:10])[CH2:6][C:5]([CH2:12][CH3:13])([CH3:11])[NH:4]1)[CH3:2].[CH3:15][N:16]=[C:17]=[O:18]>C1(C)C(C)=CC=CC=1>[CH3:15][NH:16][C:17](=[O:18])[O:10][CH:7]1[CH2:6][C:5]([CH2:12][CH3:13])([CH3:11])[NH:4][C:3]([CH2:1][CH3:2])([CH3:14])[CH:8]1[CH3:9]
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 12228异氰酸甲酯HCID 221822412,6-Diethyl-2,3,6-trimethylpiperidin-4-ol2 次

产物 1

HCID 537281202,6-Diethyl-2,3,6-trimethyl-4-piperidyl methylcarbamate收率 97.2%

试剂、催化剂与溶剂 1

HCID 7237邻二甲苯溶剂

实验过程

4.0 g of 2,6-diethyl-2,3,6-trimethyl-4-piperidinol (Compound 1) and 1.7 g of methyl isocyanate were dissolved in 6 ml of xylene and the solution was refluxed by heating for 3.5 hours. Xylene and excess methyl isocyanate were distilled off under reduced pressure. The residue was purified by column chromatography on silica gel ("60F 254", available from Merck & Co.) using a 4 : 1 by volume mixture of chloroform and methanol as eluent. The product was then distilled under reduced pressure, giving 5.0 g of Compound 66 as a pale yellow liquid (bp 145°-149° C./1.4 mmHg).

后处理

  1. temperaturethe solution was refluxed
  2. temperatureby heating for 3.5 hours
  3. distillationXylene and excess methyl isocyanate were distilled off under reduced pressure
  4. customThe residue was purified by column chromatography on silica gel ("60F 254", available from Merck & Co.)
  5. additionby volume mixture of chloroform and methanol as eluent
  6. distillationThe product was then distilled under reduced pressure

来源与证据

ORD记录
ord-55d8d52d193a4e53bd6c53b9b65fb815
来源数据集
uspto-grants-1979_02
DOI
10.6084/m9.figshare.5104873.v1
专利号
US04141883

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