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A safe and efficient route for the preparation of nitro-, dinitro-, and trinitrophenyl chloroformates

机译:一种安全高效的制备硝基,二硝基和三硝基苯基氯甲酸酯的途径

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摘要

A safe and simple method has been developed for synthesis of chloroformates derived from 2-nitrophenol, 4-nitrophenol, 2,4-dinitrophenol, 2,4,6-trinitrophenol, and pentafluorophenol, the yields being in the range of 72-96%. The method is based on a heterogeneous reaction of the substituted phenol with phosgene dissolved in dichloromethane catalyzed with solid anhydrous potassium carbonate. The synthesis of 2,4,6-trinitrophenyl chloroformate takes place only in the presence of a phase-transfer catalyst, in this case the easily recovered α,ω-dimethoxy poly(ethylene glycol) (PEG; M = 2kDa). The only waste products of the suggested synthesis of the mentioned esters are sodium chloride and potassium chloride. The method markedly reduces the explosion risk connected with drying and handling of salts of mono-, di-, and trinitrophenols and is much more environmentally friendly than the currently used methods.
机译:已开发出一种安全,简单的方法来合成由2-硝基苯酚,4-硝基苯酚,2,4-二硝基苯酚,2,4,6-三硝基苯酚和五氟苯酚衍生的氯甲酸酯,收率在72-96%的范围内。该方法基于固体无水碳酸钾催化的取代苯酚与溶于二氯甲烷的光气的非均相反应。 2,4,6-三硝基苯基氯甲酸酯的合成仅在相转移催化剂的存在下进行,在这种情况下,容易回收的α,ω-二甲氧基聚(乙二醇)(PEG; M = 2kDa)。建议合成上述酯的唯一废物是氯化钠和氯化钾。该方法显着降低了与干燥,处理单,二和三硝基酚盐有关的爆炸危险,并且比目前使用的方法对环境更加友好。

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