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乙醇 → 4-溴-6-甲基吡啶-2-羧酸乙酯

HRID 1908810
笔记
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反应方程式

HRID 1908810 反应方程式
[K+].[Br:2][C:3]1[CH:8]=[C:7]([CH3:9])[N:6]=[C:5]([C:10]([O-:12])=[O:11])[CH:4]=1.[CH2:13](O)[CH3:14]>OS(O)(=O)=O.C([O-])(O)=O.[Na+]>[CH2:13]([O:11][C:10]([C:5]1[CH:4]=[C:3]([Br:2])[CH:8]=[C:7]([CH3:9])[N:6]=1)=[O:12])[CH3:14]
参与物反应条件实验过程后处理来源与证据反应笔记

参与物

5

反应物 2

HCID 702乙醇HCID 67027109HCID 67027109,化合物

产物 1

HCID 252089814-溴-6-甲基吡啶-2-羧酸乙酯

试剂、催化剂与溶剂 2

HCID 1118四氧化硫溶剂HCID 516892碳酸氢钠溶剂

反应条件

温度
70 °C

实验过程

To a suspension of 4-bromo-6-methyl-pyridine-2-carboxylic acid potassium salt (253 mg, 0.996 mmol) in ethanol (100 mL), H2SO4 (2 mL) is added dropwise. The mixture is heated to 70° C. for 16 h before it is carefully diluted with sat. aq. NaHCO3. The mixture is extracted three times with diethyl ether. The combined org. extracts are dried over MgSO4, filtered and concentrated. The crude product is purified on prep. TLC plates with heptane:EA 3:2 to give 4-bromo-6-methyl-pyridine-2-carboxylic acid ethyl ester (105 mg) as a pale yellow oil; LC-MS: tR=0.85 min, [M+1]+=244.22.

本页导航参与物反应条件实验过程后处理来源与证据反应笔记

后处理

  1. additionis added dropwise
  2. extractionThe mixture is extracted three times with diethyl ether
  3. dry with materialextracts are dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude product is purified on prep

来源与证据

ORD记录
ord-206cfd363e164f28a5d5c20eddd7f3c9
来源数据集
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08598208B2

反应笔记

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