Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/32738
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18074/20272 (89%)
Visitors : 4368687      Online Users : 1094
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/32738


    Title: 具Bronsted-Lewis雙酸性離子液體合成與在催化Friedel–Crafts反應研究Ⅱ
    Synthesis of Bronsted-Lewis Acidic Ionic Liquids and Use as the Catalysts for Friedel–Crafts Reaction Ⅱ
    Authors: 何文岳
    Contributors: 嘉南藥理大學化妝品應用與管理系(含化妝品科技碩士班)
    Keywords: 離子液體
    Friedel–Crafts 醯化反應
    布忍司特酸
    路易士酸
    Ionic liquid
    Friedel–Crafts acrylation
    Lewis acid
    Brønsted acid
    Date: 2017
    Issue Date: 2020-11-16 15:05:22 (UTC+8)
    Abstract: 芳酮(aromatic ketones)為重要的精細化學品和中間體之芳酮(aromatic ketones)為重要的精細化學品和中間體之一,目前廣泛應用在農藥、醫藥、染料、及化妝品領域中。合成芳酮的主要方法,是利用芳香烴(arenes)在路易士酸(Lewis acid)或布忍司特酸(Brønsted acid)的催化下進行Friedel–Crafts醯化反應。在反應中,常用的催化劑有AlCl3、FeCl3、BF3等路易士酸或HCl、H2SO4等布忍司特酸,然而這些催化劑常存在無法收再利用、或是易造成設備腐蝕與環境污染的問題。本計畫以實驗室開發之雙酸性離子液體為催化劑,探討其在進行Friedel–Crafts醯化反應的影響。由實驗結果顯示:以催化劑4d,於溫度100℃下,反應2小時,合成4-甲氧基二苯甲酮(4-methoxybenzophenone)產率可達78%。且催化劑4d對水與空氣穩定,經六重複使用試驗,仍可維持良好的催化活性。
    Aromatic ketones are one of the important fine chemicals or intermediates in pesticides, pharmaceuticals, dyes, and cosmetics. Generally, aromatic ketones are synthesized via Friedel–Crafts acylation of arenes catalyzed with Lewis or Bronsted acids, such as AlCl3, FeCl3, BF3, HCl or H2SO4. However these acidic catalysts have some drawbacks like non-reusability, corrosion of equipment, and large amount of acidic liquid waste. This research studies the catalytic properties of the Bronsted-Lewis acidic ionic liquids which have synthesized in our previous work, in the Friedel–Crafts acylation reaction. It reveals, catalytic 4d is stable in water and air, and when 4d used as the catalyst, the yield of 4-methoxybenzophenone reached 78%. And it further reveals the 4d can be reused over six sequential runs without considerable loss of its initial activity.
    Relation: 計畫編號:MOST106-2221-E041-004
    計畫年度:106
    執行起迄:2017-08~2018-07
    Appears in Collections:[Dept. of Cosmetic Science and institute of cosmetic science] MOST Project

    Files in This Item:

    File Description SizeFormat
    index.html0KbHTML1261View/Open
    MOST 106-2221-E-041-004.pdf684KbAdobe PDF786View/Open


    All items in CNU IR are protected by copyright, with all rights reserved.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback