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Temperature-Residence Time Mapping

The rate of Br/Li exchange reaction, as well as that of the decomposition of the aryllithium, is dependent on temperature. The temperature-residence time map is thus useful in analyzing the reactions and optimizing the reaction conditions. In addition to the temperature-residence time map for an ethyl ester, those for other esters are also prepared (Fig. 4.8). [Pg.35]

Fig. 4.8 Temperature-residence time map for Br-Ii exchange of afkyl o-bromobenzoate followed by protonation, a t-butyl o-bromobenzoate, b isopopyl o-bromobenzoate, c ethyl o-bromobenzoate, and d methyl o-bromobenzoate... Fig. 4.8 Temperature-residence time map for Br-Ii exchange of afkyl o-bromobenzoate followed by protonation, a t-butyl o-bromobenzoate, b isopopyl o-bromobenzoate, c ethyl o-bromobenzoate, and d methyl o-bromobenzoate...
Fig. 4.14 Temperature-residence time map for I-Li exchange of alkyl p-iodobenzoates followed by protonation, a tert-butyl p-iodobenzoate, b Isopropyl p-iodobenzoate, c ethyl p-iodobenzoate, and d methyl p-iodobenzoate... Fig. 4.14 Temperature-residence time map for I-Li exchange of alkyl p-iodobenzoates followed by protonation, a tert-butyl p-iodobenzoate, b Isopropyl p-iodobenzoate, c ethyl p-iodobenzoate, and d methyl p-iodobenzoate...
Making a temperature-residence time map for such reactions is useful for controlling the reactions at optimum temperatures and with optimum residence times enabling selective synthesis of desired products with high yields. [Pg.55]


See other pages where Temperature-Residence Time Mapping is mentioned: [Pg.10]    [Pg.19]    [Pg.20]    [Pg.20]    [Pg.31]    [Pg.37]    [Pg.40]    [Pg.58]    [Pg.10]    [Pg.19]    [Pg.20]    [Pg.20]    [Pg.31]    [Pg.37]    [Pg.40]    [Pg.58]    [Pg.258]    [Pg.156]    [Pg.19]   


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