29418-59-5Relevant articles and documents
A asymmetric to P for the preparation of compounds (by machine translation)
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Paragraph 0037-0041, (2019/04/10)
The present invention discloses a non-symmetrical P-composition preparation method, in order to backward and halogenated aromatic hydrocarbons as raw material, solid alkali catalyst in dichloromethane in a two-phase system to conduct the condensation reaction, to obtain the asymmetric double-substituted jingjing passes through catalytic oxidation, to prepare the asymmetric P-compound. For the method of the invention the product yield is greater than 85% and above, the purity of the product reach 98% and above. The invention compared with the prior art, safe and convenient operation, the operating environment is greatly improved, avoiding the danger in operation of the diazotization step. The invention mild reaction conditions, good selectivity, process is easy to control, the un-reacted organic raw materials can be recycled, thereby greatly reducing the environmental protection COD treatment intensity, the product quality is stable, it is suitable for industrial production. (by machine translation)
A New and Regioselective Synthesis of Aromatic Diazene Derivatives
Neumann, Wilhelm P.,Wicenec, Christian
, p. 2297 - 2301 (2007/10/02)
A new method for the preparation of aromatic diazene derivatives 3a-l, 5, 7a, b, 9 under very mild conditions is described.The reaction of trialkylarylstannanes with nitro-substituted benzenediazonium tetrafluoroborates leads, by strict ipso substitution, to the corresponding diaryldiazenes in satisfactory to high yields.Due to the excellent leaving group quality of the stannyl group azo compounds may be prepared which are not accessible by normal electrophilic azo coupling.The products can be valuable precursors, obtained by reduction of the amines or other derivatizations, for consecutive aromatic compounds.Key Words: Aromatic substitution, electrophilic / Azo compounds, synthesis of / Diazonium compounds, aromatic, coupling reaction of, with trialkylarylstannanes / Trialkylarylstannanes, application of
BASIC PROPERTIES OF 4-ARYLAZO-PHENOLS AND 4-ARYLAZO-ANISOLES
Nesterowicz, Marianna,Korewa, Ryszard
, p. 1085 - 1092 (2007/10/02)
The conditions in which 4-arylazo-phenols and 4-arylazo-anisoles have basic properties have been studied.We have also determined the equilibrium constants of the reactions between 4-arylazo-phenols or 4-arylazo-anisoles with perchloric acid in nitromethane, acetonitrile and acetic acid.Conclusions have been drawn from the influence of the nature of solvent and substituent at the benzene ring on equilibrium constant values.