反应 #83400

反应方程式

meta-trifluoromethylphenol

sodium hydride

2,4-dichloro-6-(3-thienylmethyloxy)pyridine

water

→

4-chloro-2-(3-thienylmethyloxy)-6-(meta-trifluoromethylphenoxy)pyridine

溶剂

N,N-dimethylacetamide

N,N-dimethylacetamide

反应条件

后处理

1. 1
   温度to cool
2. 2
   其他the mixture was partitioned
3. 3
   洗涤The obtained organic layer was washed with aqueous saturated sodium chloride
4. 4
   干燥dried over anhydrous sodium sulfate
5. 5
   workup.DISTILLATIONThe solvent was distilled off
6. 6
   其他the residue was purified successively on silica gel column chromatography and on reversed phase column chromatography (Lobar column, Lichroprep RP-18, 40-63 μm, elution solvent: CH3CN/H2O=7/3(v/v)), whereby the end product
7. 7
   其他was obtained

实验过程

To a solution of meta-trifluoromethylphenol (0.28 g, 0.0018×1.0 mol) in 10 ml of dry N,N-dimethylacetamide, sodium hydride (0.077 g, (ca.60% in mineral oil), 0.0018×1.1 mol) was added. After the bubbling ceased, a solution of 2,4-dichloro-6-(3-thienylmethyloxy)pyridine (0.46 g, 0.0018 mol) in 10 ml of dry N,N-dimethylacetamide was added dropwise and the resultant solution was stirred for about 7 hours at the temperature of 160° to 170° C. After allowed to cool, water was added to the reaction solution, then the mixture was partitioned by using ethyl acetate. The obtained organic layer was washed with aqueous saturated sodium chloride and dried over anhydrous sodium sulfate. The solvent was distilled off, then the residue was purified successively on silica gel column chromatography and on reversed phase column chromatography (Lobar column, Lichroprep RP-18, 40-63 μm, elution solvent: CH3CN/H2O=7/3(v/v)), whereby the end product was obtained.

来源