首页> 外国专利> METHOD OF PRODUCTION OF N,N-BIS(2-CHLOROETHYL)TETRAHYDRO-2H-1,3,2-OXAZAPHOSPHORINE-2-AMINE 2-OXIDE

METHOD OF PRODUCTION OF N,N-BIS(2-CHLOROETHYL)TETRAHYDRO-2H-1,3,2-OXAZAPHOSPHORINE-2-AMINE 2-OXIDE

机译:N,N-双(2-氯乙基)四氢-2H-1,3,2-恶唑磷-2-氨基-2-氧化物的生产方法

摘要

The invention relates to a method of production of N,N-bis(2-chloroethyl)amino)-2-oxo-1,3,2- oxazaphosphorinane in a reaction of phosphorous oxychloride POCl3, N,N-bis(2-chloroethyl)amine, and 3-aminopropan-1-ol in a single reaction vessel, characterized by the fact that phosphorous oxychloride and N,N-bis(2-chloroethyl)amine hydrochloride are added to an inert aprotic organic solvent placed in a closed reaction vessel, in a slight molar excess in relation to phosphorous oxychloride, whereupon the mixture is cooled to temperature in the range of -15 to -10°C, and with the temperature maintained within this range and continuous stirring, the solution of 3-aminopropan-1-ol and the first portion of the auxiliary base is slowly added in an amount of 1 mole calculated as per 1 mole of 3-aminopropan-1-ol in an inert aprotic organic solvent, and subsequently, while maintaining the reaction mixture temperature in the range of -7 to -3°C the second portion of the auxiliary base is added dropwise, in an amount required for binding of HCl released during the cyclisation reaction, and after the mixture reaches temperature in the range of 15 to 20 °C it is stirred in this temperature for a period of 5 to 25 hours, whereupon, while continuously stirring, the remaining portion of the auxiliary base is added dropwise, in an amount of 2 - 2.3 moles, calculated per a theoretical amount of hydrochloride released from bis(2-chloroethyl)amine hydrochloride and released in the reaction of substitution of chlorine at the phosphorous atom in 2-chloro- tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide, and without stopping the stirring, the temperature is gradually increased from 20 to 40°C, the reaction being conducted until the conversion of the substrates is complete.
机译:本发明涉及一种在氯氧化磷POCl 的反应中生产 N,N -双(2-氯乙基)氨基)-2-氧代-1,3,2-氧杂氮代正膦烷的方法。 3 ,N,N-双(2-氯乙基)胺和3-氨基丙烷-1-醇在一个反应​​容器中,其特征在于三氯氧化磷和 N,N 将-双(2-氯乙基)胺盐酸盐加到置于密闭反应容器中的惰性非质子有机溶剂中,相对于三氯氧化磷而言摩尔浓度略有过量,随后将混合物冷却至-15至-在10°C的温度下保持连续搅拌的同时,按每1摩尔3摩尔计算的1摩尔量缓慢加入3-氨基丙-1-醇和辅助碱的第一部分的溶液。 -氨基丙-1-醇在惰性非质子有机溶剂中,随后,在保持反应混合物温度在-7至-3°C的范围内时,第二部分助剂以环化反应过程中释放的HCl结合所需的量逐滴添加一元碱,混合物达到15至20°C的温度后,在此温度下搅拌5至25小时,然后,在连续搅拌的同时,按从理论上从双(2-氯乙基)胺盐酸盐释放并在取代反应中释放的盐酸盐计算的2-2.3摩尔的量,逐滴加入剩余的辅助碱部分,为2-2.3摩尔。在2-氯-四氢-2 H -1,3,2-氧杂氮杂膦酸2-氧化物中的磷原子上生成氯,并且在不停止搅拌的情况下,温度从20°逐渐升高至40° C,进行反应直到底物的转化完成。

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