Mo-catalyzed Friedel-Crafts alkylation using alkenes under mild condition

被引:1
|
作者
Taniguchi, Nobukazu [1 ]
Kitayama, Kenji [2 ]
机构
[1] Osaka Metropolitan Univ, Dept Chem, Fac Liberal Arts Sci & Global Educ, Sakai, Osaka 5998531, Japan
[2] Daicel Corp, Mat SBU, 3-1 Ofuka Cho,Kita Ku, Osaka 5300011, Japan
关键词
Molybdenum chloride; Friedel-Crafts reaction; Hydroarylation; Alkene; Arene; INTERMOLECULAR HYDROARYLATION; ARENES; EFFICIENT; SUBSTITUTION; ETHYLENE; OLEFINS; SYSTEM;
D O I
10.1016/j.tetlet.2023.154729
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Mo-catalyzed hydroarylation of alkenes can be achieved at room temperature. The procedure can perform by using electron rich arenes, and the corresponding product is obtained regioselectively as a mixture of para- and ortho-isomers in good yield. Both aryl alkenes and aliphatic alkenes are available in the procedure. On the other hand, a reaction of allylic acetates gives the corresponding allyl arenes via leaving of acetoxy group.
引用
收藏
页数:8
相关论文
共 50 条
  • [1] Controlling the selectivity of an intramolecular Friedel-Crafts alkylation with alkenes using selenium under mild conditions
    Liao, Ming-Hong
    Zhang, Meng
    Hu, Dai-Hui
    Zhang, Rui-Han
    Zhao, Yan
    Liu, Shan-Shan
    Li, Yun-Xia
    Xiao, Wei-Lie
    Tang, E.
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2020, 18 (21) : 4034 - 4045
  • [2] Lewis Acid Catalyzed Friedel-Crafts Alkylation of Alkenes with Trifluoropyruvates
    Xiang, Bin
    Xu, Teng-Fei
    Wu, Liang
    Liu, Ren-Rong
    Gao, Jian-Rong
    Jia, Yi-Xia
    JOURNAL OF ORGANIC CHEMISTRY, 2016, 81 (09): : 3929 - 3935
  • [3] ALKYLATION OF BIPHENYL UNDER MILD FRIEDEL-CRAFTS CONDITIONS
    PRIDDY, DB
    INDUSTRIAL & ENGINEERING CHEMISTRY PRODUCT RESEARCH AND DEVELOPMENT, 1969, 8 (03): : 239 - &
  • [4] Samarium triflate-catalyzed halogen-promoted Friedel-Crafts alkylation with alkenes
    Hajra, Saumen
    Maji, Biswajit
    Bar, Sukanta
    ORGANIC LETTERS, 2007, 9 (15) : 2783 - 2786
  • [5] FRIEDEL-CRAFTS ACYLATION OF ALKENES
    GROVES, JK
    CHEMICAL SOCIETY REVIEWS, 1972, 1 (01) : 73 - &
  • [6] FRIEDEL-CRAFTS ALKYLATION PRODUCTS
    KOLB, KE
    FIELD, KW
    JOURNAL OF CHEMICAL EDUCATION, 1991, 68 (01) : 86 - 86
  • [7] FRIEDEL-CRAFTS ALKYLATION OF INDOLES
    BUDYLIN, VA
    YERMOLENKO, MS
    KOST, AN
    KHIMIYA GETEROTSIKLICHESKIKH SOEDINENII, 1978, (07): : 921 - 924
  • [8] FRIEDEL-CRAFTS ALKYLATION OF PENTAFLUOROBENZENE
    BECKERT, WF
    LOWE, JU
    JOURNAL OF ORGANIC CHEMISTRY, 1967, 32 (03): : 582 - &
  • [9] RETENTIVE FRIEDEL-CRAFTS ALKYLATION
    MASUDA, S
    NAKAJIMA, T
    SUGA, S
    JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1974, (23) : 954 - 955
  • [10] FRIEDEL-CRAFTS ALKYLATION OF PENTAFLUOROBENZENE
    BECKERT, WF
    LOWE, JU
    JOURNAL OF ORGANIC CHEMISTRY, 1967, 32 (04): : 1212 - &