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process for the production of 5, 5 '- dialkyl - 10, 10' - spiro bis phenazaverbindungen

机译:5,5'-二烷基-10,10'的制备方法-螺双苯并氮杂萘丁酮

摘要

The Specification comprises compounds of the formula: FORM:0965481/C1/1 in which Mis, Pb, Ge or Sn and R is a C1 to C5 alkyl radical. These compounds may be prepared by reacting two equivalents of 4,41-dibromo-2,21-dilithio-N-(C1-C5 alkyl) diphenylamine with one equivalent of MX4 where X is chlorine or bromine. These compounds may be reduced by means of a palladium-on-carbon catalyst in the presence of an acid acceptor to produce compounds of the formula: FORM:0965481/C1/2ALSO:The Specification comprises compounds of the formula: FORM:0965481/C3/1 in which M is Si, Pb, Ge or Sn (see also Division C2) and R is a C1 to C5 alkyl radical. These compounds may be prepared by reacting 2 equivalents of 4,41-dibromo-2, 21-dilithio-N-(C1-C5 alkyl) diphenylamine with one equivalent of MX4 where X is chlorine or bromine. These compounds may be reduced by means of a palladium-on-carbon catalyst in the presence of an acid acceptor to produce compounds of the formula: FORM:0965481/C3/2 Examples describe the preparation of (1) (A). 2, 21, 4, 41-tetrabromo -N- ethyl-diphenylamine. 1 (B) 2, 21, 8, 81-tetrabromo-5, 51-diethyl-10, 101-spirobiphenylaziline and 5,51-diethyl-10, 101h spirobiphenylphenazaline.
机译:该说明书包括下式的化合物:其中Mis,Pb,Ge或Sn和R是C1-C5烷基。这些化合物可通过使两当量的4,41-二溴-2,21-二硫代-N-(C1-C5烷基)二苯胺与一当量的MX4反应制得,其中X为氯或溴。这些化合物可以在酸受体存在下借助于碳载钯催化剂还原以产生下式的化合物: ALSO:说明书包括下式的化合物: :0965481 / C3 / 1>其中M是Si,Pb,Ge或Sn(也参见C2部分),R是C1-C5烷基。这些化合物可以通过使2当量的4,41-二溴-2、21-二硫代-N-(C1-C5烷基)二苯胺与一当量的MX4反应来制备,其中X是氯或溴。这些化合物可以在酸受体存在下借助于碳载钯催化剂还原以产生下式的化合物:实施例描述了(1)(A)的制备。 2、21、4、41-四溴-N-乙基-二苯胺。 1(B)2、21、8、81-四溴5、51-二乙基-10、101-螺联苯并苯胺和5,51-二乙基-10、101 h螺二苯基苯并氮杂。

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