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碳酸二乙酯 → 2-(2-氯吡啶-4-基)乙酸乙酯

HRID 911069
笔记
打印预览

反应方程式

HRID 911069 反应方程式
C(NC(C)C)(C)C.C([Li])CCC.[Cl:13][C:14]1[CH:19]=[C:18]([CH3:20])[CH:17]=[CH:16][N:15]=1.[C:21](=O)([O:25]CC)[O:22][CH2:23][CH3:24].CN(C)P(N(C)C)(N(C)C)=O>C1COCC1>[Cl:13][C:14]1[CH:19]=[C:18]([CH2:20][C:21]([O:22][CH2:23][CH3:24])=[O:25])[CH:17]=[CH:16][N:15]=1
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

7

反应物 5

HCID 7766碳酸二乙酯HCID 7912DiisopropylamineHCID 12679六甲基磷酰三胺HCID 772482-氯-4-甲基吡啶HCID 178418339正丁基锂

产物 1

HCID 577092362-(2-氯吡啶-4-基)乙酸乙酯收率 75.5%

试剂、催化剂与溶剂 1

HCID 8028
四氢呋喃
溶剂
2 次

反应条件

温度
-78 °C

实验过程

In a 1000 mL round-bottom flask, diisopropylamine (80.21 mL, 567.5 mmol) was combined with THF (250 mL) and cooled to −78° C. Butyllithium (227.0 mL, 567.5 mmol) (2.5M in hexane) was added and the mixture was stirred for 30 minutes. 2-Chloro-4-methylpyridine (36.20 g, 283.8 mmol) in THF (100 mL) was added, and the mixture was stirred for 2 hours. A mixture of diethyl carbonate (37.82 mL, 312.1 mmol) and hexamethylphosphoramide (54.31 mL, 312.1 mmol) was added, and the mixture was stirred at −78° C. for one hour and then stirred at ambient temperature. The reaction was quenched with 25% ammonium chloride solution and extracted twice with ethyl acetate. The combined organic extracts were washed with brine, dried and evaporated. The crude oil was purified by silica gel chromatography, eluting with 5% ethyl acetate/hexane to provide the desired product as clear oil (42.75 g, 75.47% yield).

后处理

  1. stirringthe mixture was stirred for 2 hours
  2. additionwas added
  3. stirringthe mixture was stirred at −78° C. for one hour
  4. stirringstirred at ambient temperature
  5. customThe reaction was quenched with 25% ammonium chloride solution
  6. extractionextracted twice with ethyl acetate
  7. washThe combined organic extracts were washed with brine
  8. customdried
  9. customevaporated
  10. customThe crude oil was purified by silica gel chromatography
  11. washeluting with 5% ethyl acetate/hexane

来源与证据

ORD记录
ord-0996133c30114a7799e347736b3bccf5
来源数据集
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08022222B2

反应笔记

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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