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S-Triazine prodn. from formamidine acetate and orthoformate - avoiding use of hydrocyanic acid and giving high yield of pure prod.

机译:S-三嗪产品由甲form乙酸盐和原甲酸盐制成-避免使用氢氰酸,并获得高产率的纯产品。

摘要

Prodn. of s-triazine (I) comprises reacting formamidine acetate (II) with =2, pref. 2-2.4 moles of a 1-6C alkyl orthoformate (III) at 120, pref. 130-160 degrees C. The volatile reaction prods. and then the (I) formed are distilled out, and (I) sepd. conventionally from the combined distillates. Pref. (II) is made by reacting NH4 acetate and an orthoformate and is used without further purification. (I) is used in synthesis of heterocycles. In an example, reaction of 20.8 g (II) and 58.8 g. triethyl orthoformate at 135-140 degrees C gave an 80.6% yield of pure (I).
机译:产品s-三嗪(I)的混合物包括乙酸甲form(II)与> = 2,优选地。 2-120摩尔> 120的原甲酸1-6C烷基酯(III),优选。 130-160℃。挥发性反应产物。然后蒸馏出形成的(I),和(I)sepd。通常从合并的馏出物中提取。首选(II)通过使NH 4乙酸盐和原甲酸酯反应而制得,无需进一步纯化即可使用。 (I)用于杂环的合成。在一个实例中,反应为20.8g(II)和58.8g。在135-140℃下,原甲酸三乙酯得到80.6%的纯(I)收率。

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