首页> 外国专利> Process for the preparation of 6-methyl-3,4-dihydro-1,2,3-oxathiazin-4-one-2,2-dioxide and non-toxic salts thereof and lithium and ammonium salts of acetoacetamide-N-sulfonic acid

Process for the preparation of 6-methyl-3,4-dihydro-1,2,3-oxathiazin-4-one-2,2-dioxide and non-toxic salts thereof and lithium and ammonium salts of acetoacetamide-N-sulfonic acid

机译:制备6-甲基-3,4-二氢-1,2,3-恶唑嗪-4-one-2,2-二氧化物及其无毒盐以及乙酰乙酰胺-N-磺酸锂和铵盐的方法

摘要

6-Methyl-3,4-dihydro-1,2,3-oxathiazin-4-one 2,2-dioxide is prepared by (a) reacting, in an inert organic solvent, a salt of sulfamic acid, which is at least partially soluble therein, with at least approximately the equimolar amount of an acetoacetylating agent, in the presence of an amine or phosphine catalyst, and by cyclizing the acetoacetamide-N-sulfonate which is formed in this reaction, or the free sulfonic acid, (b) by the action of at least approximately the equimolar amount of SO3, where appropriate in an inert inorganic or organic solvent, to give 6-methyl-3,4-dihydro-1,2,3-oxathiazin-4-one 2,2-dioxide, which is produced in the form of the acid in this reaction; it is possible, if desired, to obtain from the acid form (c) the appropriate salts by neutralization with bases. The non-toxic salts-in particular the potassium salt-are valuable synthetic sweeteners.
机译:6-甲基-3,4-二氢-1,2-,3-恶唑嗪-4-酮2,2-二氧化物的制备方法是:(a)在惰性有机溶剂中,使至少为氨基磺酸的氨基磺酸盐反应在胺或膦催化剂的存在下,至少部分等摩尔量的乙酰乙酰化剂在其中部分溶解,并通过环化在该反应中形成的乙酰乙酰胺-N-磺酸盐或游离磺酸,(b ),至少在惰性无机或有机溶剂中,至少约等摩尔量的SO3作用,得到6-甲基-3,4-二氢-1,2,3-氧杂噻嗪-4-酮2,2 -二氧化物,在该反应中以酸的形式产生;如果需要,可以通过用碱中和从酸形式(c)获得适当的盐。无毒盐,特别是钾盐,是有价值的合成甜味剂。

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