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Bromomesitylene Bromonaphthalene

Grignard reagent from -amyl bromide, 16, 41 from benzyl chloride, 10, 4 17, 89 from bromomesitylene, 11, 66 from a-bromonaphthalene, 11, 80 from 2-bromopentane, 11,84 from -butyl bromide, 15,11 from ethyl bromide, 11, 98 17, 48 from iso propyl bromide, IS, 48... [Pg.54]

Bromination of arenesp- This reagent brominates activated arenes at room temperature in DMF/H2O (phenol — tribromophenol, 89% yield). Less reactive aromatics are brominated by 1 in the presence of HgCL as catalyst (mesitylene — 2-bromomesitylene, 76% yield). Polycyclic arenes are brominated by 1 in refluxing acetic acid (naphthalene — 1-bromonaphthalene, 65% yield). [Pg.100]

See other pages where Bromomesitylene Bromonaphthalene is mentioned: [Pg.92]    [Pg.97]    [Pg.47]    [Pg.47]    [Pg.47]    [Pg.50]    [Pg.154]    [Pg.48]   
See also in sourсe #XX -- [ Pg.8 , Pg.10 , Pg.11 , Pg.14 ]

See also in sourсe #XX -- [ Pg.8 , Pg.10 , Pg.11 , Pg.14 ]



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