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    • 1. 发明授权
    • Preparation of secondary and tertiary 2-methyl-1, 5-pentanediamines
    • 二级和叔级2-甲基-1,5-戊二胺的制备
    • US06198002B1
    • 2001-03-06
    • US09324715
    • 1999-06-03
    • Karsten EllerBernd FiegeStefan RittingerEberhard Fuchs
    • Karsten EllerBernd FiegeStefan RittingerEberhard Fuchs
    • C07C20948
    • C07C211/09C07C209/48
    • A process for preparing a secondary or tertiary 2-methyl-1,5-pen-tanediamine of the formula I where R1 and R2 are H, C1-C20-alkyl, C3-C8-cycloalkyl, aryl, C7-C20-arylalkyl, where the radicals R1 and R2 may bear substituents selected from the group consisting of C1-C20-alkyl, C1-C20-alkoxy, C6-C20-aryloxy and hydroxy, and R1 and R2 are not simultaneously hydrogen, or R1 and R2 are together an unsubstituted or C1-C20-alkyl- and/or C1-C20-alkoxy-substituted C3-C7-alkylene chain which may, if desired, be interrupted by one or two O or NR3 groups, where R3 is H or C1-C20-alkyl comprises reacting 2-methylglutarodinitrile with a primary or secondary amine of the formula R1R2NH and hydrogen at from 50 to 250° C. and pressures of from 0.5 to 35 MPa in the presence of an oxidic supported catalyst comprising one or more noble metals which has been treated with hydrogen at from 50 to 300° C. for at least 0.5 hour before use. The compound 1,5-bis(dimethylamino)-2-methylpentane is also claimed.
    • 制备式I其中R 1和R 2的仲或叔2-甲基-1,5-辛烷二胺的方法是H,C 1 -C 20 - 烷基,C 3 -C 8 - 环烷基,芳基,C 7 -C 20 - 芳烷基,其中 基团R 1和R 2可以具有选自C 1 -C 20 - 烷基,C 1 -C 20 - 烷氧基,C 6 -C 20 - 芳氧基和羟基的取代基,并且R 1和R 2不同时为氢,或者R 1和R 2一起为未取代或未取代的 C 1 -C 20烷基 - 和/或C 1 -C 20 - 烷氧基取代的C 3 -C 7 - 亚烷基链,如果需要,可以被一个或两个O或NR 3基团中断,其中R 3是H或C 1 -C 20烷基, - 甲基戊二腈与式R1R2NH的伯胺或仲胺和50-250℃的氢气和0.5-35MPa的压力在包含一种或多种已经用氢处理过的贵金属的氧化载体催化剂存在下 在使用前至少0.5小时,从50至300℃。 还要求化合物1,5-双(二甲基氨基)-2-甲基戊烷。
    • 5. 发明授权
    • Preparation of peralkylated amines
    • 全烷基化胺的制备
    • US5463130A
    • 1995-10-31
    • US395596
    • 1995-02-28
    • Tom WitzelEberhard FuchsHorst Zimmermann
    • Tom WitzelEberhard FuchsHorst Zimmermann
    • B01J23/44B01J23/58B01J23/63C07B61/00C07C209/48C07C209/60C07C211/09C07C213/02C07C215/08C08G18/18C08G59/68
    • C07C209/48C08G18/1808C08G18/1825C08G59/686
    • A process for the preparation of peralkylated amines of the general formula I ##STR1## in which R.sup.1, R.sup.2 denote C.sub.1 -C.sub.200 alkyl, C.sub.3 -C.sub.8 cycloalkyl, C.sub.4 -C.sub.20 alkylcycloalkyl, C.sub.4 -C.sub.20 cycloalkylalkyl, C.sub.2 -C.sub.20 alkoxyalkyl, aryl, C.sub.7 -C.sub.20 alkylaryl, C.sub.7 -C.sub.20 aralkyl, C.sub.2 -C.sub.8 hydroxyalkyl, C.sub.2 -C.sub.8 mercaptoalkyl, C.sub.8 -C.sub.20 phenoxyalkyl, C.sub.2 -C.sub.8 aminoalkyl, C.sub.2 -C.sub.8 (NHR.sup.4)alkyl, C.sub.2 -C.sub.8 (NR.sup.4 R.sup.5)alkyl or together form a saturated or unsaturated C.sub.2 -C.sub.6 alkylene chain optionally mono- to tri-substituted by C.sub.1 -C.sub.4 alkyl and optionally interrupted by oxygen or nitrogenX denotes a C.sub.2 -C.sub.20 alkylene or C.sub.2 -C.sub.20 alkenylene or C.sub.4 -C.sub.8 cycloalkylene chain optionally mono- to penta-substituted by R.sup.3, C.sub.1 -C.sub.8 alkyl, C.sub.1 -C.sub.8 alkoxy, C.sub.1 -C.sub.8 dialkylamino, phenoxy, diphenylamino and/or C.sub.2 -C.sub.8 alkoxycarbonyl,A denotes hydrogen, C.sub.1 -C.sub.20 alkyl, C.sub.3 -C.sub.8 cycloalkyl, C.sub.4 -C.sub.20 alkylcycloalkyl, C.sub.4 -C.sub.20 cycloalkylalkyl, C.sub.2 -C.sub.20 alkoxyalkyl, aryl, C.sub.7 -C.sub.20 alkylaryl, C.sub.7 -C.sub.20 aralkyl, C.sub.1 -C.sub.20 alkoxy, hydroxy, C.sub.1 -C.sub.20 hydroxyalkyl, amino, C.sub.1 -C.sub.20 alkylamino, C.sub.2 -C.sub.20 dialkylamino, C.sub.3 -C.sub.12 alkenyleneamino, C.sub.3 -C.sub.8 cycloalkylamino, arylamino, aryl-C.sub.1 -C.sub.12 alkylamino, halogen, mercapto, C.sub.2 -C.sub.20 alkenylenoxy, C.sub.3 -C.sub.8 cycloalkoxy and aryloxyR.sup.3 denotes CH.sub.2 --NR.sup.1 R.sup.2,R.sup.4, R.sup.5 denote C.sub.1 -C.sub.20 alkylby the reaction of a nitrile of the general formula IIA--X--CN (II),in which R.sup.1, R.sup.2, R.sup.4, R.sup.5, X and A have the aforementioned meanings and R.sup.3 stands for --CH.sub.2 --NR.sup.1 R.sup.2 or cyano, with a secondary amine of the general formula III ##STR2## and hydrogen at temperatures ranging from 50.degree. to 250.degree. C. and pressures ranging from 5 to 350 bar in the presence of a catalyst, wherein the catalyst used is palladium on an oxidic support.
    • 制备通式I(I)的全烷基胺的方法,其中R 1,R 2表示C 1 -C 20烷基,C 3 -C 8环烷基,C 4 -C 20烷基环烷基,C 4 -C 20环烷基烷基,C 2 -C 20烷氧基烷基,芳基,C 7 -C 20烷基芳基 C 7 -C 20烷基,C 2 -C 8羟烷基,C 2 -C 8巯基烷基,C 8 -C 20苯氧烷基,C 2 -C 8氨基烷基,C 2 -C 8(NHR 4)烷基,C 2 -C 8(NR 4 R 5)烷基或一起形成饱和或不饱和的C 2 -C 6亚烷基链, 被C1-C4烷基三取代并且任选地被氧或氮中断X表示任选被R 3,C 1 -C 8烷基,C 1 -C 8烷氧基,C 1 -C 8烷氧基取代的C 2 -C 20亚烷基或C 2 -C 20亚烯基或C 4 -C 8亚烷基链, C 2 -C 20烷基氨基,苯氧基,二苯基氨基和/或C 2 -C 8烷氧基羰基,A表示氢,C 1 -C 20烷基,C 3 -C 8环烷基,C 4 -C 20烷基环烷基,C 4 -C 20环烷基烷基,C 2 -C 20烷氧基烷基,芳基,C 7 -C 20烷基芳基,C 7 -C 20芳烷基,C 1 -C 20烷氧基, 羟基,C 1 -C 20羟烷基,氨基,C 1 -C 20烷基氨基,C 2 -C 20二烷基氨基,C 3 -C 12亚烯基氨基, C 3 -C 8环烷基氨基,芳基氨基,芳基-C 1 -C 12烷基氨基,卤素,巯基,C 2 -C 20烯基烯氧基,C 3 -C 8环烷氧基和芳氧基R 3表示CH 2 -NR 1 R 2,R 4,R 5表示通过通式II的腈反应的C 1 -C 20烷基 -CN(II),其中R1,R2,R4,R5,X和A具有上述含义,R3代表-CH2-NR1R2或氰基,与通式III的仲胺(III)和 氢气在50至250℃的温度和5至350巴的压力范围内,在催化剂存在下,其中使用的催化剂是氧化载体上的钯。
    • 6. 发明授权
    • Preparation of caprolactam
    • 己内酰胺的制备
    • US06683179B2
    • 2004-01-27
    • US10258941
    • 2002-10-29
    • Peter BasslerDieter BaumannRolf-Hartmuth FischerEberhard FuchsJohann-Peter MelderFrank Ohlbach
    • Peter BasslerDieter BaumannRolf-Hartmuth FischerEberhard FuchsJohann-Peter MelderFrank Ohlbach
    • C07D20108
    • C07D201/08
    • A process for the preparation of caprolactam is provided, wherein a) a mixture (I) containing 6-aminocapronitrile and water is reacted in the gas phase, in the presence of a catalyst, to give a mixture (II) containing caprolactam, ammonia, water, high-boiling components and low-boiling components, b) ammonia is then removed from the mixture (II) to give a mixture (III) containing caprolactam, water, high-boiling components and low-boiling components, c) water is then removed from the mixture (III) to give a mixture (IV) containing caprolactam, high-boiling components and low-boiling components, and d) a solid (V) containing caprolactam is then obtained from the mixture (IV) by crystallization, the proportion by weight of caprolactam in the solid (V) being greater than in the mixture (IV).
    • 提供了制备己内酰胺的方法,其中a)含有6-氨基己腈和水的混合物(I)在催化剂存在下在气相中反应,得到含己内酰胺,氨,水的混合物(II) ,高沸点组分和低沸点组分,b)然后从混合物(II)中除去氨,得到含有己内酰胺,水,高沸点组分和低沸点组分的混合物(III),c)然后将水 从混合物(III)中除去,得到含有己内酰胺,高沸点组分和低沸点组分的混合物(IV),然后通过结晶从混合物(IV)获得含有己内酰胺的固体(V),比例 的固体(V)中的己内酰胺的量大于混合物(IV)中的。
    • 7. 发明授权
    • Preparation of caprolactam
    • 己内酰胺的制备
    • US06677449B2
    • 2004-01-13
    • US10258942
    • 2002-10-29
    • Peter BasslerDieter BaumannRolf-Hartmuth FischerEberhard FuchsJohann-Peter MelderFrank Ohlbach
    • Peter BasslerDieter BaumannRolf-Hartmuth FischerEberhard FuchsJohann-Peter MelderFrank Ohlbach
    • C07D20102
    • C07D201/08C07D201/16
    • A process for the preparation of caprolactam is provided, wherein a) a mixture (I) containing 6-aminocapronitrile and water is reacted in the liquid phase, in the presence of a catalyst, to give a mixture (II) containing caprolactam, ammonia, water, high-boiling components and low-boiling components, b) ammonia is then removed from the mixture (II) to give a mixture (III) containing caprolactam, water, high-boiling components and low-boiling components, c) water is then removed from the mixture (III) to give a mixture (IV) containing caprolactam, high-boiling components and low-boiling components, and d) a solid (V) containing caprolactam is then obtained from the mixture (IV) by crystallization, the proportion by weight of caprolactam in the solid (V) being greater than in the mixture (IV).
    • 提供了制备己内酰胺的方法,其中a)含有6-氨基己腈和水的混合物(I)在液相中在催化剂存在下反应,得到含有己内酰胺,氨,水的混合物(II) ,高沸点组分和低沸点组分,b)然后从混合物(II)中除去氨,得到含有己内酰胺,水,高沸点组分和低沸点组分的混合物(III),c)然后将水 从混合物(III)中除去,得到含有己内酰胺,高沸点组分和低沸点组分的混合物(IV),然后通过结晶从混合物(IV)获得含有己内酰胺的固体(V),比例 的固体(V)中的己内酰胺的量大于混合物(IV)中的。
    • 8. 发明授权
    • Pyrogenic titanium dioxide
    • 热原二氧化钛
    • US06663844B1
    • 2003-12-16
    • US09486488
    • 2000-02-29
    • Eberhard FuchsKlemens Flick
    • Eberhard FuchsKlemens Flick
    • C01G2307
    • B01J21/063B01J37/06C07D201/08
    • Shaped materials useful as catalyst for preparing cyclic lactams by reacting aminocarbonitriles with water in the liquid phase in a fixed bed reactor and which have no soluble constituents under the reaction conditions, comprising pyrogenic titanium dioxide as essential constituent, these compositions being obtainable by shaping the pyrogenic titanium dioxide into shaped articles and, before or after the shaping, treating the pyrogenic titanium dioxide with from 0.1 to 30% by weight, based on the pyrogenic titanium dioxide, of an acid in which pyrogenic titanium dioxide is sparingly soluble.
    • 成型材料可用作制备环状内酰胺的催化剂,其通过在固定床反应器中使氨基碳腈与液相中的水反应,并且在反应条件下不含可溶性成分,其包含热解二氧化钛作为必要组分,这些组合物可通过将热解法 二氧化钛成型制品,并且在成形之前或之后,以热解二氧化钛为基准,以热解二氧化钛为基准,以热解二氧化钛微溶于其中的酸为基础,以0.1至30重量%的量处理热解二氧化钛。