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Synthesis of 2-Aryloxymethylbenzonitriles from 2-Cyanobenzyl Chloride

机译:由2-氰基苄基氯合成2-芳氧基甲基苄腈

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摘要

Fourteen 2-Aryloxymethylbenzonitriles were synthesized from 2-cyanobenzyl chloride and various substituted phenols with potassium carbonate as a base in N,N-dimethyl formamide at 80-110 °C in good to excellent yields. The products, 13 of which are new, were characterized by melting points, 'H nuclear magnetic resonance spectroscopy and electron impact mass spectroscopy. 2-Cyanobenzyl chloride is thus a better alternative to more costly and less atom economical bromo analogue or chloro- or bromobenzoate.
机译:在80-110°C下,由N-N-二甲基甲酰胺中的碳酸钾为碱,由2-氰基苄基氯和各种取代的苯酚与2-氰基苄基氯和各种取代的苯酚合成十四个2-芳氧基甲基苯甲腈。该产品中有13种是新产品,其特征在于熔点,'H核磁共振波谱和电子冲击质谱。因此,2-氰基苄基氯是成本更高,原子经济性更低的溴代类似物或氯代或溴代苯甲酸酯的更好替代品。

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