首页> 外国专利> Chloroprene prepn. from (3,4)-dichloro-butene-(1) - by dehydrochlorination with alkali in presence of thio-diphenylamine and (2,6)-di-tert. butyl-(para)-cresol

Chloroprene prepn. from (3,4)-dichloro-butene-(1) - by dehydrochlorination with alkali in presence of thio-diphenylamine and (2,6)-di-tert. butyl-(para)-cresol

机译:氯丁二烯(3,4)-二氯丁烯-(1)-通过在硫代-二苯胺和(2,6)-二叔胺存在下用碱脱氯化氢而得。丁基-(对)甲酚

摘要

The process comprises dehydrochlorinating 3,4-dichlorobutene-1 (I) with alkali in the presence of thiodiphenylamine (II) and 2,6-di-tert-butyl-p-cresol (II). Effective amt. of (II) is 0.01-1 wt. % pref. 0.05-0.5 wt. % to (I). Amt. of (III) is pref. 0.01-1 wt. %, esp. pref. 0.05-0.5 wt. % to (I). Pref. the stabilisers are added to (I) beforehand. Used amt. of alkali is eqiv. to that of (I). When (II) and (III) are present in the reaction mixt. polymer formation is prevented effectively and as a result, operation becomes extremely stable and can be continued for a long periods.
机译:该方法包括在硫代二苯胺(II)和2,6-二叔丁基对甲酚(II)存在下用碱将3,4-二氯丁烯-1(I)脱氯化氢。有效的amt。 (II)的重量为0.01-1重量%。 %偏好0.05-0.5重量%(I)。 Amt。 (III)的首选项0.01-1重量%,特别是偏好0.05-0.5重量%(I)。首选预先将稳定剂加入(I)中。二手的。碱的当量。与(I)相同。当反应混合物中存在(II)和(III)时。有效地防止了聚合物的形成,结果,操作变得非常稳定并且可以长期持续。

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