“…Adjustments to the depth of immersion were made so that a maximum amount of agitation in the liquid was noted, and the flask was clamped firmly3 in place, A heavy precipitate of lithium bromide is formed as the reaction proceeds, Bromobenzene reacts similarly, although less vigorously, to afford biphenyl. THF is a better solvent than ether in these reactions (6), although it is often more convenient to use the latter. The cross-coupling of alkyl and aryl halides (Wurtz-Fittig reaction) may be carried out similarly (7).…”
Bromopropane, bromobutane, and bromopentane were found to react vigorously with lithium in ether solution when bombarded with ultrasound to give hexane, octane, and decane, but little reaction took place in the absence of sonication.
“…Adjustments to the depth of immersion were made so that a maximum amount of agitation in the liquid was noted, and the flask was clamped firmly3 in place, A heavy precipitate of lithium bromide is formed as the reaction proceeds, Bromobenzene reacts similarly, although less vigorously, to afford biphenyl. THF is a better solvent than ether in these reactions (6), although it is often more convenient to use the latter. The cross-coupling of alkyl and aryl halides (Wurtz-Fittig reaction) may be carried out similarly (7).…”
Bromopropane, bromobutane, and bromopentane were found to react vigorously with lithium in ether solution when bombarded with ultrasound to give hexane, octane, and decane, but little reaction took place in the absence of sonication.
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