会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明授权
    • Method for producing purified epoxy compound
    • 纯化环氧化合物的制备方法
    • US5892065A
    • 1999-04-06
    • US892198
    • 1997-07-14
    • Suketoshi TsukamotoTakami OnoHisao IkedaMotohiko Hidaka
    • Suketoshi TsukamotoTakami OnoHisao IkedaMotohiko Hidaka
    • C07D301/27C07D301/32C07D303/16C07D301/02C07D405/12
    • C07D303/16C07D301/32C08G59/025
    • A 2,3-epoxypropyl derivative or a 2-methyl-2,3-epoxypropyl derivative of a compound having carboxyl groups or amido groups is produced as a purified product having an epoxide equivalent of 1.0 to 1.1 times the theoretical epoxide equivalent of the derivative, an ionic halogen content of 10 ppm or less, transparency when molten and a stability against increase in the epoxide equivalent when stored at 150.degree. C. for 24 hours, by a process comprising steps (A) reacting 1.2 to 60 mol of an epihalohydrin or a 2-methyl-epihalohydrin with 1 mol of active hydrogen atoms of the carboxyl or amido group of the compound in the presence of a particular catalyst, thereby forming a reaction product containing a 2-hydroxy-3-halopropyl derivative or a 2-hydroxy-2-methyl-3-halopropyl derivative, (B) dehydrohalogenating the derivative by adding to the reaction product a sufficient amount of an alkali metal hydroxide thereby forming a final slurry containing the 2,3-epoxypropyl derivative of the 2-methyl-2,3-epoxypropyl derivative and the alkali metal halide, (C) washing the final slurry or a liquid product formed by removing the alkali metal halide from the final slurry thereby forming a refined liquid containing the derivative, and (D) removing by evaporation the epihalohydrin or the 2-methyl-epihalohidrin from the refined liquid, thereby forming the 2,3-epoxypropyl derivative or the 2-methyl-2,3-epoxypropyl derivative as the purified product.
    • 制备具有羧基或酰胺基的化合物的2,3-环氧丙基衍生物或2-甲基-2,3-环氧丙基衍生物作为纯化产物,其环氧当量为衍生物的理论环氧当量的1.0-1.1倍 ,离子卤素含量为10ppm以下,当熔融时的透明度和在150℃下储存24小时时的环氧当量增加的稳定性,通过包括以下步骤的方法:(A)使1.2至60摩尔的表卤代醇 或具有1摩尔化合物的羧基或酰胺基的活性氢原子的2-甲基 - 表卤代醇在特定催化剂的存在下反应,从而形成含有2-羟基-3-卤代丙基衍生物或2-羟基-3-卤代丙基衍生物的反应产物, 羟基-2-甲基-3-卤代丙基衍生物,(B)通过向反应产物中加入足够量的碱金属氢氧化物脱卤化氢,从而形成含有2-甲基-3-氯丙基衍生物的2,3-环氧丙基衍生物的最终浆液, 2,3-环氧丙基衍生物和碱金属卤化物,(C)洗涤最终浆料或通过从最终浆料中除去碱金属卤化物形成的液体产物,从而形成含有该衍生物的精制液体,(D)通过蒸发除去 来自精制液体的表卤代醇或2-甲基 - 表卤代醇,由此形成2,3-环氧丙基衍生物或2-甲基-2,3-环氧丙基衍生物作为纯化产物。