CAS: 1504-58-1; 3-Phenylprop-2-Yn-1-Ol

该化合物是含有分子式C9H8O的苯代丙基酒精,该化合物具有终端烷基和氢氧基组,使其成为有机合成的多功能中间体,其反应性三重结合使得它能够参与点击化学,Sonogashira相交和其他交叉反应,而氢氧基组则允许进一步功能化.该苯基环可增强芳香替代途径的稳定性和影响再活动性.该化合物对于建造复杂的分子手杖的制药和农用化学研究特别有用.其定义明确的结构和再活性特征使它成为热循环和精细化学合成的宝贵建筑块.

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合成工艺路线路线简述

  • 合成目标产物 3-Phenyl-2-Propyn-1-Ol 主要起始原料 α-Bromocinnamaldehyde
  • (文献来源)合成步骤主要原料 α-Bromocinnamaldehyde
二苯基亚砜置于potassium Phosphate,Copper(L) Iodide,二(三叔丁基膦)钯体系中,用 二氯甲烷,N,N-二甲基甲酰胺 用作溶剂,化学反应 42.0H,反应生成3-苯基-2-丙炔-1-醇
参考文献:使用芳基ulf盐作为交叉偶联伙伴的sonogashira反应
标题:使用芳基ulf盐作为交叉偶联伙伴的sonogashira反应
摘要:三芳基ulf,烷基和氟烷基(二芳基)ulf和芳基(二烷基)ulf三氟甲磺酸盐已成功用作sonogashira反应中的交叉偶联新家族,如芳基重氮盐,二芳基碘鎓盐和四苯基phosph盐.发现末端炔烃在室温下在pd-和cu-共催化下与三芳基(或三氟甲磺酸(2,2,2-三氟乙基)二苯基mild轻度反应,以高达> 99%的收率获得相应的芳基炔.该方案代表在pd / Cu催化的sonogashira反应中首次使用芳基ulf盐作为交叉偶联伴侣.
Doi:10.1021/acs.Orglett.7B02764

海关参考信息

专利信息


专利号:US-2007082923-A1
优先权日:2005-10-05
标题:Process for the synthesis of compounds for selectin inhibition
发明人:WANG YOUCHU
权利人:WANG YOUCHU
摘要:The present teachings relate to the field of anti-inflammatory substances, and more particularly to the preparation of compounds that act as antagonists of the mammalian adhesion proteins known as selecting. In some embodiments, the present teachings provide methods for preparing compounds for treating selectin-mediated disorders that have the formula VI: n n nwherein R 1 , R 2 , R 3 , p, and q are defined herein.

专利号:WO-2022268526-A1
优先权日:2021-06-21
标题 :Process for the synthesis of propargylic alcohol by reacting formaldehyde with acetylene in the presence of a homogeneous copper catalyst

专利号:US-11383220-B1
优先权日:2018-02-26
标题 :Method and material for synthesis and purification by use of a coated solid substrate
发明人:HAMMOND GERALD B; XU BO
权利人:Faster Chemistry LLC
摘要:The method and materials of this invention make possible substantially faster techniques for organic-aqueous extractions and routine chemical reactions work-ups. The inventive material uses silicone elastomer-coated glass powders, magnetic powders, and sponges as absorbents to extract organic products from an aqueous mixture. After separation from the mixture, these different forms now loaded with organic products can serve as a convenient input for flash chromatographic separations or other processing. With these techniques, tedious liquid-liquid extractions are replaced by a simple solid filtration or transfer and emulsion formation is eliminated. These versatile sorbents can also be used for larger scale work-ups, various extractions of organics from an aqueous solution (e.g., water purification) or gas phase and various analytical or other applications.

专利号:CN-115745866-B
优先权日:2022-11-08
标 题:Preparation of phthalimidyl ionic liquid and method for catalytic synthesis of alpha-alkyl unsaturated cyclic carbonate by using same

专利号:CN-110218214-B
优先权日:2018-03-02
标题:A kind of benzo[3,3,1]oxa-bridged ring ketal derivative and its synthesis method and application

专利号:CN-115110104-A
优先权日:2022-04-06
标 题 :Photoelectrochemical synthesis method of alpha, alpha-dichloro aryl ketone compound
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主要参考文献

参考标题:Investigations On Gold‐catalyzed Thioalkyne Activation Toward Facile Synthesis Of Ketene Dithioacetals
作者:Xiaohan Ye,Jin Wang,Shengtao Ding,Seyedmorteza Hosseyni,Lukasz Wojtas,Novruz G. Akhmedov,Xiaodong Shi |发布日期:2017.8.4
摘要:From A Gold‐associated Thioketene Intermediate. Based On This Interesting Mechanistic Insight, A Gold(I)‐catalyzed Thioether Addition To Thioalkynes Was Developed As A Novel Approach To Prepare Ketene Dithioacetals With Good Yields And High Efficiency.

合成参考文献


摘要:Alonso, D. A.; Nájera, C., Science of Synthesis, (2010) 45, 224.
摘要:Amatore, M.; Aubert, C.; Malacria, M.; Petit, M., Science of Synthesis Knowledge Updates, (2012) 3, 66.
摘要:Weibel, J.-M.; Blanc, A.; Pale, P., Science of Synthesis Knowledge Updates, (2018) 1, 73.
摘要:Hou, X.-L.; Peng, X.-S.; Yeung, K.-S.; Wong, H. N. C., Science of Synthesis Knowledge Updates, (2011) 2, 281.
摘要:Hou, X.-L.; Peng, X.-S.; Yeung, K.-S.; Wong, H. N. C., Science of Synthesis Knowledge Updates, (2011) 2, 272.
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