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1-Bromo-3-phenylpropane: Benzene,

Bromo-3-phenylpropane Benzene, (3-bromopropyl)- (8,9) (637-59-2) Triphenylphosphine Phosphine, triphenyl- (8,9) (603-35-0)... [Pg.81]

Phenylpropyl bromide ALDRICH 1-Bromo-3-phenylpropane Benzene,... [Pg.98]

BROMO-2-FLUORO-2-PHENYLPROPANE BENZENE, (2-BROMO-1-FLUORO-... [Pg.310]

Bromo-2-fluoro-2-phenylpropane Benzene, (2-bromo-1-fluoro-1-methylethyl)- (9) (59974-27-5)... [Pg.164]

A novel ionic liquid methodology for pyrrole C-alkylation is described (Equation 136) <20050L1231>. The pyrrole alkylation is achieved with various simple alkyl halides (1-bromopentadecane, l-(bromomethyl)-, l-(3-chloropropyl)- and l-(3-iodopropyl)benzenes, 2-(2-bromoethyl)- and 2-(3-bromopropyl)naphthalenes) and mesylates (3-phenylpropyl-, l-methyl-3-phenylpropyl-, 2-(2-naphthyl)ethyl- and 3-(2-naphthyl)propyl methanesulfonates) selectively at C(2)- and C(5)-positions in good yields with minimal by-products under relatively mild conditions in various ionic liquids. 2-(3-Phenylpropyl)pyrrole 569 was synthesized from pyrrole and l-bromo-3-phenylpropane in a mixed solvent system, [Bmim][SbF6] and MeCN, in 81% yield at 115°C for 44h with 5% yield of dialkylated compound. [Pg.131]

See other pages where 1-Bromo-3-phenylpropane: Benzene, is mentioned: [Pg.154]    [Pg.139]    [Pg.314]    [Pg.158]    [Pg.154]    [Pg.139]    [Pg.314]    [Pg.158]    [Pg.1100]    [Pg.1263]    [Pg.1267]   
See also in sourсe #XX -- [ Pg.2 , Pg.75 , Pg.155 ]

See also in sourсe #XX -- [ Pg.2 , Pg.75 , Pg.155 ]

See also in sourсe #XX -- [ Pg.2 , Pg.75 , Pg.155 ]



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1- Bromo-2-phenylpropane

2- Phenylpropanal

3-Phenylpropan

Bromo-benzene

Phenylpropane

Phenylpropanes

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