1,10-BIS(4-NITROPHENYL)-1,3,5,7,9-DECAPENTAENE AND PRODUCTION THEREOF

    公开(公告)号:JPS63270643A

    公开(公告)日:1988-11-08

    申请号:JP10549087

    申请日:1987-04-28

    Applicant: RICOH KK

    Abstract: NEW MATERIAL:1,10-Bis(4-nitrophenyl)-1,3,5,7,9-decapentaene shown by formula I. USE:An intermediate for a bisazo compound useful as an organic photoconductive material suitable for not only high-speed copying machines but also electrophotographic sensitized substance showing practically high sensitivity for laser printer, especially a lamination type sensitized substance. PREPARATION:A bisphosphonium salt shown by formula II (R is phenyl or alkyl; X is halogeno ion) is reacted with trans-4-nitrocinnamic aldehyde in the presence of a basic catalyst at room temperature - about 100 deg.C to give a compound shown by formula I. The nitro group of the compound is reduced with an amino group and then diazotized to give a bis(diazonium) salt, which is coupled with a coupler to give a bisazo compound shown by formula III (Ar is coupler residue).

    Nitration of chlorobenzene
    125.
    发明专利
    Nitration of chlorobenzene 失效
    氯化硼的硝化

    公开(公告)号:JPS5724331A

    公开(公告)日:1982-02-08

    申请号:JP9690480

    申请日:1980-07-17

    Abstract: PURPOSE: When chlorobenzene is nitrated with nitric acid in the presence of sulfuric acid, the reaction temperature is set in a specific range to facilitate the temperature control and produce an isomer mixture of nitrochlorobenzene with no side-reactions, which is used as an intermediate of dyes.
    CONSTITUTION: Chlorobenzene is nitrated with nitric acid in the presence of sulfuric acid, preferably of 70W90% concentration, at 85W150°C to produce an isomer mixture of nitrochlorobenzene. The nitration is effected preferably by dropping a mixed acid of sulfuric and nitric acids to a suspension of chlorobenzene in sulfuric acid. The weight ratio of sulfuric acid to chlorobenzene is preferably 1.5W3.0.
    COPYRIGHT: (C)1982,JPO&Japio

    Abstract translation: 目的:当硫酸在硝酸中硝化氯苯时,将反应温度设定在特定范围内,以便温度控制,并产生无副反应的硝基氯苯的异构体混合物,其用作中间体 染料。 构成:氯苯在硝酸氯苯的异构体混合物的存在下,在硫酸存在下,优选浓度为70-90%,在85-150℃下硝化。 硝化最好通过将硫酸和硝酸的混合酸滴加到氯苯在硫酸中的悬浮液中进行。 硫酸与氯苯的重量比优选为1.5-3.0。

    PREPARATION OF LOWER NITROPARAFFINS
    126.
    发明专利

    公开(公告)号:JPS56169649A

    公开(公告)日:1981-12-26

    申请号:JP7374080

    申请日:1980-06-03

    Abstract: PURPOSE:To obtain the titled compound in high selectivity and in high yield, by reacting an inexpensive lower alkyl chloride as a raw material which exists in an organic phase with an alkali metal salt of nitric acid in a solid phase using a catalyst transferring between phases under mild conditions. CONSTITUTION:A 1-3C lower alkyl chloride is present directly in the absence of a solvent, or is dissolved in a hydrophobic organic solvent so that it exists in the organic phase, while an alkali metal salt of nitric acid is made to exist in solid state directly in a solid phase. The both compounds are reacted using a catalyst transferring between the organic and solid phases, to give a corresponding lower nitroparaffin. A large cyclic polyether, e,g., dibenz-18-crown-6, etc. or a crypstand shown by the formula (l, m, and n are 0-2) may be used as the catalyst transferring between the phases. The reaction temperature is preferably 5-90 deg.C, the pressure is normal pressure to 5kg/cm G, and, if necessary, it may be reduced pressure.

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