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PREPARATION OF 2,3-DICHLORO-1,4-NAPHTHOQUINONE

机译:2,3-二氯-1,4-萘醌的制备

摘要

PURPOSE:In preparing the titled compound by chlorinating 1,4-naphthoquinone, to make filtrate into a solvent and to circulate it for use without causing problems of corrosion of device, etc., and to improve purity and yield, by adding ammonia to the reaction solution in order to remove hydrogen chloride, etc. dissolved in the reaction solution after the reaction completion, neutralizing it. CONSTITUTION:In producing 2,3-dichloro-1,4-naphthoquinone by chlorinating 1,4-naphthoquinone, after the reaction is over, the reaction solution is neutralized with ammonia.Confirmation of the neutralization point is carried out by oxidation-reduction potential. When the oxidation-reduction potential becomes 500mV--100mV, preferably 450mV-300mV, it is considered to reach the neutralization point. After the neutralization, a solid component containing the titled compound is filtered, and the filtrate is circulated and used as a solvent for the next reaction. Before the neutralization with ammonia is carried out, preferably aeration is done. As for condition, the neutralization is carried out at 85-95 deg.C for 30-60min at the same temperature as that in the chlorination.
机译:用途:在通过氯化1,4-萘醌制备标题化合物时,将滤液制成溶剂并循环使用,而不会引起设备腐蚀等问题,并通过向其中添加氨来提高纯度和收率。反应完成后,为了除去溶解在反应溶液中的氯化氢等,将其中和。组成:氯化1,4-萘醌生产2,3-二氯-1,4-萘醌的过程中,反应结束后用氨水中和反应溶液,通过氧化还原电位确定中和点。当氧化还原电位变为500mV--100mV,优选450mV-300mV时,认为达到中和点。中和后,过滤包含标题化合物的固体组分,并使滤液循环并用作下一步反应的溶剂。在用氨中和之前,优选进行通气。至于条件,在与氯化反应相同的温度下,在85-95℃下进行中和30-60分钟。

著录项

  • 公开/公告号JPS6118742A

    专利类型

  • 公开/公告日1986-01-27

    原文格式PDF

  • 申请/专利权人 NITSUPOU KAGAKU KK;FUSOU KAGAKU KOGYO KK;

    申请/专利号JP19840139114

  • 发明设计人 SUZUKI HISASHI;YABE HIROTA;

    申请日1984-07-06

  • 分类号C07C46/00;C07C45/00;C07C50/24;C07C67/00;

  • 国家 JP

  • 入库时间 2022-08-22 07:47:59

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