1972
DOI: 10.1002/chin.197203103
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ChemInform Abstract: EINFLUSS DES LOESUNGSMITTELS AUF DEN MECHANISMUS DER WURTZ‐FITTIG‐RK.

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“…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).…”
mentioning
confidence: 99%
“…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).…”
mentioning
confidence: 99%