首页> 外国专利> process for the preparation of a mixture of the trans - décahydronaphtalène hydroperoxide.the cis alpha - and beta décahydronaphtol cis and cis alpha and cis beta décahydronaphtalène ketones.

process for the preparation of a mixture of the trans - décahydronaphtalène hydroperoxide.the cis alpha - and beta décahydronaphtol cis and cis alpha and cis beta décahydronaphtalène ketones.

机译:制备反式-十二氢萘萘过氧化氢的混合物的方法。顺式α-和β-二氢萘酚的顺式和顺式α-和顺式β-萘二氢萘酮的酮。

摘要

Trans-9-decahydronaphthalene peroxide and cis-a - and cis-b -decahydronaphthalene ketones and alcohols are produced by reacting pure decahydronaphthalene (as defined) with O2 or an O2-containing gas at 80 to 170 DEG C. "Pure decahydronaphthalene" is defined as decahydronaphthalene, consisting of at least 90% of cisdecahydronaphthalene, from which other substances contained in technically pure decahydronaphthalene have been removed. When the process is carried out at 80 to 110 DEG C. for 24 to 72 hours, the conversion kept below 30%, and water produced by secondary reactions immediately removed from the reaction zone, a product rich in trans-9-decahydronaphthalene peroxide is formed. When the process is carried out at 130 DEG to 170 DEG C. for 4 to 24 hours, the main reaction products are cis-a - and cis-b - decahydronaphthalene ketones and alcohols.
机译:反式-9-十氢萘过氧化物和顺式-a-和顺式-b-十氢萘酮和醇是通过使纯十氢萘(定义)与O 2或含O 2的气体在80至170℃下反应而制得的。“纯十氢萘”为术语“十氢化萘”定义为十氢萘,由至少90%的顺癸基萘组成,从中除去了技术纯正十氢化萘中所含的其他物质。当该方法在80至110℃下进行24至72小时时,转化率保持在30%以下,并且由次级反应产生的水立即从反应区中除去,富含反式-9-十氢萘过氧化物的产物为形成。当该方法在130至170℃下进行4至24小时时,主要反应产物是顺式-α-和顺式-b-十氢萘酮和醇。

著录项

  • 公开/公告号BE605718A

    专利类型

  • 公开/公告日1961-11-03

    原文格式PDF

  • 申请/专利号BE19610605718

  • 发明设计人

    申请日1961-07-04

  • 分类号1C07CA;

  • 国家 BE

  • 入库时间 2022-08-23 18:51:51

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号