Process for isolating dinitronaphthalenes
    112.
    发明授权
    Process for isolating dinitronaphthalenes 失效
    分离食品的方法

    公开(公告)号:US4053526A

    公开(公告)日:1977-10-11

    申请号:US672689

    申请日:1976-04-01

    CPC classification number: C07C201/16

    Abstract: 1,5- AND 1,8-DINITRONAPHTHALENES ARE ISOLATED FROM MIXTURES OF ISOMETRIC DINITRONAPHTHALENES AT LEAST CONTAINING THE SAME. The mixture of isomers is treated successively with a more polar solvent and a less polar aromatic solvent for dinitronaphthalenes thereby dissolving the mixture of isomers except for 1,5-dinitronaphthalenes which remains largely undissolved in the more polar solvent. The residual mixture of isomers is subsequently treated, after removal of the more polar solvent, with a less polar aromatic solvent at elevated temperatures in which 1,8-dinitronaphthalenes remains as a largely insoluble residue.

    Esterification of nitrobenzoic acids
    114.
    发明授权
    Esterification of nitrobenzoic acids 失效
    硝基苯甲酸酯化

    公开(公告)号:US3948972A

    公开(公告)日:1976-04-06

    申请号:US414891

    申请日:1973-11-12

    CPC classification number: C07C201/12 C07C201/16 C07C227/04 C07C227/40

    Abstract: Glycerol esters of nitrobenzoic acid are prepared by heating a mixture of a nitrobenzoic acid and glycerol in the presence of a catalytic quantity of an acid esterification catalyst which is soluble in the reaction medium at the reaction temperature. An entraining liquid having a boiling point above 100.degree.C is also present in the raction mixture. The reaction mixture is heated to a temperature above 100.degree.C so that liberated water is separated by azeotropic distillation. Surprisingly good yields are obtained using these reaction conditions.

    Abstract translation: 在催化量的酸酯化催化剂存在下,在反应温度下可溶于反应介质的硝基苯甲酸和甘油的混合物中,制备硝基苯甲酸的甘油酯。 沸点高于100℃的夹带液也存在于反应混合物中。 将反应混合物加热至高于100℃的温度,以便通过共沸蒸馏分离释放的水。 令人惊讶的是,使用这些反应条件获得良好的收率。

    Process for the purification of p-nitrophenol
    115.
    发明授权
    Process for the purification of p-nitrophenol 失效
    纯化对硝基苯酚的方法

    公开(公告)号:US3933929A

    公开(公告)日:1976-01-20

    申请号:US360097

    申请日:1973-05-14

    Inventor: Gilbert Colovray

    CPC classification number: C07C201/16 C07C201/08 C07C205/22

    Abstract: In a purification process for p-nitrophenol obtained by nitration of phenol, separation of crude nitrophenols, steam distillation to remove o-nitrophenol, and cooling the broth obtained when it contains more than 0.5% sodium bisulphite and is at pH 5.4 to 6.4 to deposit crystals of p-nitrophenol, an improvement consists in stirring the crystals with water at 55.degree.-85.degree.C to give a mixture containing 10-40% excess of p-nitrophenol over the solubility at that temperature, separating the upper layer of p-nitrophenol in water obtained, cooling it to 40.degree.-50.degree.C and separating the layer of water in p-nitrophenol, cooling the latter to below 30.degree.C and collecting the crystals deposited.

    Abstract translation: 在通过硝化苯酚获得的对硝基苯酚的纯化方法中,分离粗的硝基酚,蒸汽蒸馏以除去邻硝基苯酚,并且当其含有超过0.5%的亚硫酸氢钠时,获得的培养基冷却并且在pH 5.4至6.4下沉积 对硝基苯酚的晶体的改进在于在55℃-85℃下用水搅拌晶体,得到含有10-40%过量的对硝基苯酚的混合物超过该温度下的溶解度, 硝基苯酚在水中的溶液中,冷却至40°-50℃,分离出对硝基苯酚的水层,将其冷却至30℃以下,收集晶体沉积物。

    Recovery of purified 1-nitroanthraquinone
    117.
    发明授权
    Recovery of purified 1-nitroanthraquinone 失效
    回收纯化的1-硝基蒽醌

    公开(公告)号:US3923845A

    公开(公告)日:1975-12-02

    申请号:US38483473

    申请日:1973-08-02

    Applicant: BASF AG

    CPC classification number: C07C201/16 C07C205/47

    Abstract: A process for the recovery of 1-nitroanthraquinone in a purified state from a nitroanthraquinone mixture containing it by treatment with a base in the presence of an initiator such as nitrite, halide, thiocyanate, alcoholate or phenolate ions in an organic solvent. A 1-nitroanthraquinone is obtained which is essentially pure or contains only small quantities of isomers and dinitroanthraquinones.

    Abstract translation: 通过在有机溶剂中在引发剂如亚硝酸盐,卤化物,硫氰酸盐,醇化物或酚盐离子存在下用碱处理,从含有它的硝基蒽醌混合物中回收纯化状态的1-硝基蒽醌的方法。 得到基本上纯的或仅含有少量异构体和二硝基蒽醌的1-硝基蒽醌。

    Nitration of benzoic acid esters
    118.
    发明授权
    Nitration of benzoic acid esters 失效
    苯甲酸酯的硝化

    公开(公告)号:US3819680A

    公开(公告)日:1974-06-25

    申请号:US4153470

    申请日:1970-05-28

    Applicant: GAF CORP

    Abstract: MONONITRO DERIVATIVES OF BENZOIC ACID, AND MONO- AND DICHLORO-BENZOIC ACID, ARE PRODUCED ECONOMICALLY AND IN GOOD YIELD BY NITRATION OF BENZOIC ACID OR CHLORO- OR DICHLORO-BENZOIC ACID ESTERS, PREFERABLY A LOWER ALKYL ESTER, WITH A MIXTURE OF NITRIC ACID AND SULFURIC ACID, OR OLEUM CONTAINING UP TO THE THEORETICAL OF SULFUR TRIOXIDE REQUIRED TO COMBINE WITH THE WATER FORMED IN NITRATION, AT A TEMPERATURE OF ABOUT 10* C, TO ABOUT 80* C. THE THUS PRODUCED MONONITRO ESTERS MAY BE HYDROLYZED TO THE CORRESPONDING MONONITRO-ACID.

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