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Process for the manufacture of N-(beta- diorganodithiophosphorylethyl) aryl and alkyl sulfonamides

机译:N-(β-二有机二硫代磷酰基乙基)芳基和烷基磺酰胺的制备方法

摘要

N-(beta-diorganodithiophosphorylethyl) aryl and alkyl sulfonamides are prepared by a process comprising reacting a compound having the formula R. sup.1 SO.sub.2 X with 2-aminoethyl hydrogen sulfate and an aqueous solution of M.sup.1 OH, and reacting the resulting product with a compound having the formula ##STR1## In the above description, R. sup.1 is selected from the group consisting of C.sub.1 -C.sub.10 alkyl, halo- substituted C.sub.1 -C.sub. 10 alkyl, phenyl, halo-substituted phenyl, nitro-substituted phenyl, and naphthyl; R.sup.2 and R.sup.3 are independently selected from the group consisting of C.sub.1 -C.sub.10 alkyl and C.sub.1 -C.sub.10 alkoxy; X is selected from the group consisting of chloride, bromide, and iodide; and M.sup.1 and M.sup. 2 are independently selected from the group consisting of lithium, sodium, potassium, ammonium, and tri-substituted ammonium wherein the substituents are independently C.sub.1 -C.sub.10 alkyl.
机译:N-(β-二有机二硫代磷酰基乙基)芳基和烷基磺酰胺是通过以下方法制备的:使具有式R. sup.1 SO 2 X的化合物与2-氨基乙基硫酸氢盐和M.sup.1的水溶液反应OH,并使所得产物与具有式## STR1 ##的化合物反应。在以上描述中,R.up.1选自C 1 -C 10烷基,卤代-。取代的C.sub.1 -C.sub。 10个烷基,苯基,卤素取代的苯基,硝基取代的苯基和萘基; R 2和R 3独立地选自C 1 -C 10烷基和C 1 -C 10烷氧基; X选自氯化物,溴化物和碘化物;和M.sup.1和M.sup。 2独立地选自锂,钠,钾,铵和三取代的铵,其中取代基独立地是C 1 -C 10烷基。

著录项

  • 公开/公告号US4117043A

    专利类型

  • 公开/公告日1978-09-26

    原文格式PDF

  • 申请/专利权人 STAUFFER CHEMICAL COMPANY;

    申请/专利号US19770836322

  • 发明设计人 LLEWELLYN W. FANCHER;JEFFREY D. ROBBINS;

    申请日1977-09-26

  • 分类号C07F9/165;C07F9/32;C07F9/40;

  • 国家 US

  • 入库时间 2022-08-22 21:25:29

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