Butyrolactone-preparation process
    1.
    发明授权
    Butyrolactone-preparation process 失效
    丁内酯制备工艺

    公开(公告)号:US5962700A

    公开(公告)日:1999-10-05

    申请号:US11607

    申请日:1998-02-12

    CPC分类号: C07D315/00

    摘要: A process for the preparation of butyrolactones of the formula I ##STR1## where the substituents R.sup.1 and R.sup.2 are hydrogen, alkyl or hydroxyalkyl groups, or aryl and trialkylsilyl groups, if appropriate carrying inert: substituents, is described in which an alkyne of the formula IIR.sup.1 --C.tbd.C--R.sup.2 IIwhere the substituents have the meanings indicated above, is reacted under reducing conditions at elevated pressure and elevated temperature with carbon monoxide CO and hydrogen in the presence of a transition metal catalyst or with carbon monoxide and water in the presence of a transition metal catalyst.

    摘要翻译: PCT No.PCT / EP96 / 03472 Sec。 371日期1998年2月12日 102(e)日期1998年2月12日PCT 1996年8月6日PCT PCT。 公开号WO97 / 07111 日期1997年2月27日描述了制备式I的丁内酯的方法,其中取代基R 1和R 2是氢,烷基或羟基烷基,或芳基和三烷基甲硅烷基,如果适用的话带有惰性:取代基,其中描述了炔 其中取代基具有上述含义的式IIR1-C 3BOND C-R2II在还原条件下在升高的压力和升高的温度下与一氧化碳CO和氢在过渡金属催化剂或一氧化碳和水的存在下反应 过渡金属催化剂的存在。

    Preparation of acetylenic compounds
    2.
    发明授权
    Preparation of acetylenic compounds 失效
    制备炔属化合物

    公开(公告)号:US5723678A

    公开(公告)日:1998-03-03

    申请号:US631095

    申请日:1996-04-12

    摘要: Acetylenic compounds of the general formula I R.sup.1 --C.tbd.C--CHR.sup.2 --CH.sub.2 --X I where the substituents have the following meanings: R.sup.1 hydrogen, unsubstituted or substituted alkyl or aryl; R.sup.2 hydrogen or C.sub.1 -C.sub.4 -alkyl; X CN; COOR.sup.3 where R.sup.3 is C.sub.1 -C.sub.6 -alkyl or benzyl; C(O)R.sup.4 where R.sup.4 is hydrogen or C.sub.1 -C.sub.4 -alkyl, are prepared by reacting an alkyne of the formula II R.sup.1 --C.tbd.C--H II with an .alpha.,.beta.-unsaturated compound of the formula III R.sup.2 HC.dbd.CH--X III in the presence of a homogeneous rhodium-phosphine catalyst, in a process wherein a catalyst with a bidentate or tridentate phosphine compound is used.

    摘要翻译: 通式ⅠR1-C3BOC C-CHR2-CH2-XI的乙炔化合物,其中取代基具有下列含义:R 1氢,未取代或取代的烷基或芳基; R2氢或C1-C4-烷基; X CN; COOR 3,其中R 3是C 1 -C 6 - 烷基或苄基; 其中R 4是氢或C 1 -C 4 - 烷基的C(O)R 4是通过使式IIR 1 -C 3 3BOND C-HII的炔与式III的α,β-不饱和化合物反应来制备的。R2HC = CH-XIII 在均相铑 - 膦催化剂的存在下,在其中使用具有二齿或三齿膦化合物的催化剂的方法中。

    Preparation of N-alkenyl carboxamides
    3.
    发明授权
    Preparation of N-alkenyl carboxamides 失效
    N-烯基甲酰胺的制备

    公开(公告)号:US5710331A

    公开(公告)日:1998-01-20

    申请号:US548724

    申请日:1995-10-26

    CPC分类号: C07C231/08

    摘要: Preparation of N-alkenyl carboxamides of the general formula I ##STR1## in which the radicals R.sup.1 to R.sup.4 independently stand for hydrogen or for aliphatic, cycloaliphatic, or aromatic radicals, which optionally carry inert substituents, wherein an amide of the general formula II ##STR2## in which the radical R.sup.1 has the above meaning, and a carbonyl compound of the general formula III ##STR3## in which the radicals R.sup.2 to R.sup.4 have the above meanings, are caused to react in the presence of a base, said reaction being either a) carried out in the presence of a carboxylic acid derivative of the general formula IV ##STR4## in which the radical R.sup.5 stands for hydrogen or an alkyl or aryl group and X is a halogen, alkoxy, or carboxylalkyl radical, or b) continued in the presence of a carboxylic acid derivative of the formula IV, and the amide of the formula I is isolated.

    摘要翻译: 其中基团R 1至R 4独立地代表氢或用于任选地带有惰性取代基的脂族,脂环族或芳族基团的通式I(I)的N-烯基甲酰胺的制备,其中一般的酰胺 其中基团R 1具有上述含义的式II(II)和其中基团R 2至R 4具有上述含义的通式III(III)的羰基化合物进行反应 碱的存在,所述反应是a)在通式IV(IV)的羧酸衍生物存在下进行,其中基团R 5代表氢或烷基或芳基,X是 卤素,烷氧基或羧基烷基,或b)在式Ⅳ的羧酸衍生物存在下连续进行,分离式Ⅰ的酰胺。

    Preparation of N-akenylcarbamic esters
    4.
    发明授权
    Preparation of N-akenylcarbamic esters 失效
    N-烯基氨基甲酸酯的制备

    公开(公告)号:US5639890A

    公开(公告)日:1997-06-17

    申请号:US705682

    申请日:1996-08-29

    CPC分类号: C07C269/06 C07D263/22

    摘要: N-Alkenylcarbamic esters of the general formula I ##STR1## where at least one of the R.sup.1 radicals is hydrogen and the second R.sup.1 radical is hydrogen or C.sub.1 -C.sub.4 --alkyl, the R.sup.2 radical is an aliphatic, cycloaliphatic, araliphatic or aromatic radical which can be linked to the R.sup.3 radical to form a 2- to 10-membered bridge, and the R.sup.3 radical is an aliphatic, cycloaliphatic or aromatic radical, from an alkenyl carboxylate of the general formula II ##STR2## where R.sup.1 has the abovementioned meaning, and R.sup.4 is hydrogen, an aliphatic, cycloaliphatic or aromatic radical, and a carbamic ester of the general formula III ##STR3## where the R.sup.2 and R.sup.3 radicals have the abovementioned meanings, are prepared by reacting the starting compounds in the presence of a base.

    摘要翻译: 其中至少一个R 1基团是氢且第二个R 1基团是氢或C 1 -C 4 - 烷基,R 2基团是脂族,环脂族,芳脂族或芳族基团的通式I的N-烯丙基氨基甲酸酯 其可以连接到R 3基团以形成2-至10-元桥,并且R 3基团是脂肪族,脂环族或芳族基团,其通式II的烯基羧酸酯其中R1具有上述 并且R 4是氢,脂族,脂环族或芳族基团,和通式III的氨基甲酸酯,其中R 2和R 3基团具有上述含义,是通过使起始化合物在 一个基地

    Preparation of N-alkenylureas
    6.
    发明授权
    Preparation of N-alkenylureas 失效
    N-烯基脲的制备

    公开(公告)号:US5739398A

    公开(公告)日:1998-04-14

    申请号:US675585

    申请日:1996-07-03

    CPC分类号: C07C273/1863

    摘要: A process for preparing N-alkenylureas of the general formula I ##STR1## where R.sup.1 and R.sup.2 are hydrogen, C.sub.1 - to C.sub.40 -alkyl, C.sub.2 - to C.sub.40 -alkenyl, C.sub.3 - to C.sub.20 -cycloalkyl, C.sub.4 - to C.sub.20 -alkylcyc1oalkyl, C.sub.4 - to C.sub.20 -cycloalkylalkyl, aryl, C.sub.7 - to C.sub.20 -alkylaryl or C.sub.7 - to C.sub.20 -aralkyl, or aryl, C.sub.7 - to C.sub.20 -alkylaryl or C.sub.7 - to C.sub.20 -aralkyl which are mono- to pentasubstituted by C.sub.1 - to C.sub.8 -alkyl, C.sub.1 - to C.sub.8 -alkoxy or halogen, together are a C.sub.2 - to C.sub.10 -alkylene chain which is unsubstituted or mono- to hexasubstituted by C.sub.1 - to C.sub.8 -alkyl, and R.sup.3 and R.sup.4 are hydrogen or C.sub.1 - to C.sub.8 -alkyl, by reaction of ureas of the general formula II ##STR2## where R.sup.1 and R.sup.2 have the abovementioned meanings, with an alkenyl carboxylate of the general formula III ##STR3## where R.sup.3 and R.sup.4 have the abovementioned meanings and R.sup.5 is hydrogen, C.sub.1 - to C.sub.40 -alkyl, C.sub.3 - to C.sub.20 -cycloalkyl, C.sub.4 - to C.sub.20 -alkylcycloalkyl, aryl, C.sub.7 - to C.sub.20 -alkylaryl, C.sub.7 - to C.sub.20 -aralkyl, or aryl or C.sub.7 - to C.sub.20 -aralkyl which is mono- to trisubstituted by C.sub.1 - to C.sub.8 -alkyl, at from 0.degree. to 180.degree. C. and from 0.01 to 10 bar, by carrying out the reaction in the presence of a base is described.

    摘要翻译: 制备通式I(I)的N-烯基脲的方法,其中R 1和R 2是氢,C 1至C 40烷基,C 2至C 40链烯基,C 3 -C 20环烷基,C 4 -C 20 - 烷基环烷基,C 4 -C 20 - 环烷基烷基,芳基,C 7 -C 20 - 烷基芳基或C 7 -C 20 - 芳烷基,或被C 1 - 单取代成五取代的芳基,C 7 -C 20 - 烷基芳基或C 7 -C 20 - 芳烷基 -C 8 - 烷基,C 1 -C 8 - 烷氧基或卤素,一起是未被取代或被C 1〜C 8 - 烷基单取代或六取代的C 2〜C 10 - 亚烷基链,R 3和R 4是氢或C 1〜 通过其中R1和R2具有上述含义的通式II的脲(II)与通式III的烯基羧酸酯(III)的反应,其中R 3和R 4具有 R 5是氢,C 1 -C 40 - 烷基,C 3 -C 20 - 环烷基,C 4 -C 20 - 烷基环烷基,芳基,C 7 -C 20烷基芳基,C 7 -C 20 - 芳烷基或芳基或C 7 - 被单 - 三取代的C 20 - 芳烷基 描述了通过在碱的存在下进行反应的0至180℃和0.01至10巴的C 1 -C 8烷基。

    Preparation of N-alkenylcarboxamides
    7.
    发明授权
    Preparation of N-alkenylcarboxamides 失效
    N-链烯基酰胺的制备

    公开(公告)号:US5654478A

    公开(公告)日:1997-08-05

    申请号:US513739

    申请日:1995-08-10

    CPC分类号: C07C231/08

    摘要: N-Alkenylcarboxamides of the formula I ##STR1## where at least one of the radicals R.sup.1 is hydrogen, the second radical R.sup.1 is hydrogen or C.sub.1 -C.sub.4 -alkyl and R.sup.2 is hydrogen or an aliphatic, cycloaliphatic or aromatic radical, are prepared by reacting an alkenyl carboxylate of the formula II ##STR2## where R.sup.1 has the abovementioned meanings and R.sup.3 is hydrogen or an aliphatic, cycloaliphatic or aromatic radical, and a carboxamide of the general formula III ##STR3## where R.sup.2 has the abovementioned meanings, in the presence of a base.

    摘要翻译: 其中至少一个基团R 1为氢,第二基团R 1为氢或C 1 -C 4 - 烷基且R 2为氢或脂族,脂环族或芳族基团的式I的N-烯基甲酰胺通过 使式II其中R 1具有上述含义并且R 3是氢或脂族,脂环族或芳族基团的式II的烯基羧酸酯和具有上述含义的通式III的羧酰胺反应, 在一个基地的存在。

    Preparation of monovinyl ethers
    9.
    发明授权
    Preparation of monovinyl ethers 失效
    单乙烯基醚的制备

    公开(公告)号:US5723685A

    公开(公告)日:1998-03-03

    申请号:US548739

    申请日:1995-10-26

    CPC分类号: C07C41/08 C07C41/54

    摘要: The preparation of monovinyl ethers of the general formula I ##STR1## in which A stands for a chemical bond or for a methylene or ethylene group, the radicals R.sup.1 and R.sup.2 independently stand for hydrogen, alkyl, cycloalkyl, or aryl groups or R.sup.1 and R.sup.2 together form a C.sub.3 -C.sub.5 alkylene bridging member, by the reaction of a diol of the general formula II ##STR2## in which the variables have the above meanings, with acetylene in the presence of a base, in which the reaction is carried out at 150.degree.-250.degree. C. under an acetylene partial pressure of 5-25 bar until 40-80% of the diol has been converted, at which point the reaction is stopped and the monovinyl ether of the formula I is isolated.

    摘要翻译: 制备通式I的单乙烯基醚(I)其中A代表化学键或亚甲基或亚乙基,基团R 1和R 2分别代表氢,烷基,环烷基或芳基或 R 1和R 2一起形成C 3 -C 5亚烷基桥连体,通过其中变量具有上述含义的通式II的二醇(II)与乙炔在碱的存在下反应,其中 反应在150-250℃,乙炔分压为5-25巴下进行,直到二醇的40-80%转化为止,此时反应停止,式I的单乙烯基醚 是孤立的

    Preparation of N-alkenylazoles
    10.
    发明授权
    Preparation of N-alkenylazoles 失效
    N-链烯基唑的制备

    公开(公告)号:US5646293A

    公开(公告)日:1997-07-08

    申请号:US675588

    申请日:1996-07-03

    摘要: A process for preparing N-alkenylazoles of the general formula I ##STR1## where X is CH--R.sup.6 or nitrogen,R.sup.1 and R.sup.2 are hydrogen or C.sub.1 - to C.sub.8 -alkyl,R.sup.3,R.sup.4,R.sup.5 and R.sup.6 are hydrogen, C.sub.1 - to C.sub.40 -alkyl, C.sub.2 - to C.sub.40 -alkenyl, C.sub.3 - to C.sub.20 -cycloalkyl, C.sub.4 - to C.sub.20 -alkylcycloalkyl, C.sub.4 - to C.sub.20 -cycloalkylalkyl, aryl, C.sub.7 - to C.sub.20 -alkylaryl or C.sub.7 - to C.sub.20 -aralkyl, or aryl, C.sub.7 - to C.sub.20 -alkylaryl or C.sub.7 - to C.sub.20 -aralkyl which are mono- to pentasubstituted by C.sub.1 - to C.sub.8 -alkyl, C.sub.1 - to C.sub.8 -alkoxy or halogen, or R.sup.3 and R.sup.4 or R.sup.4 and R.sup.5 or R.sup.5 and R.sup.6 together are a C.sub.2 - to C.sub.10 -alkylene chain which is unsubstituted or mono- to hexasubstituted by C.sub.1 - to C.sub.8 -alkylby reaction of azoles of the general formula II ##STR2## where X, R.sup.3, R.sup.4 and R.sup.5 have the abovementioned meanings, with an alkenyl carboxylate of the general formula III ##STR3## where R.sup.1 and R.sup.2 have the abovementioned meanings and R.sup.7 is hydrogen, C.sub.1 - to C.sub.40 -alkyl, C.sub.3 - to C.sub.20 -cycloalkyl, C.sub.4 - to C.sub.20 -alkylcycloalkyl, aryl, C.sub.7 - to C.sub.20 -alkylaryl, C.sub.7 - to C.sub.20 -aralkyl, or aryl or C.sub.7 - to C.sub.20 -aralkyl which is mono- to trisubstituted by C.sub.1 - to C.sub.8 -alkyl, at from 0.degree. to 180.degree. C. and from 0.01 to 10 bar, which comprises carrying out the reaction in the presence of a base and of a quaternary salt, is described.

    摘要翻译: 制备通式I(I)的N-烯基唑的方法,其中X是CH-R6或氮,R1和R2是氢或C1-至C8-烷基,R3,R4,R5和R6是氢, C 1至C 40 - 烷基,C 2至C 40 - 烯基,C 3 -C 20 - 环烷基,C 4至C 20 - 烷基环烷基,C 4 -C 20 - 环烷基烷基,芳基,C 7 -C 20烷基芳基或C 7 -C 20 - 芳烷基 ,或被C 1〜C 8 - 烷基,C 1 -C 8 - 烷氧基或卤素单 - 五取代的芳基,C 7〜C 20 - 烷基芳基或C 7〜C 20 - 芳烷基,或者R 3和R 4或R 4和R 5或R 5 和R6一起是C2至C10亚烷基链,其未被取代或被C 1 -C 8 - 烷基单取代或被六取代的通式II(II)的唑类,其中X,R 3,R 4和R 5 具有上述含义,具有通式III(III)的烯基羧酸酯,其中R 1和R 2具有上述含义,并且R 7是氢,C 1至C 40烷基,C 3 -C 20环烷基,C 4至 C20-烷基环烷基,芳基,C7-至C20-烷基芳基,C7-至C20-芳基 烷基或芳基或被C 1 -C 8烷基单取代三取代的C 7 -C 20 - 芳烷基,其中0至180℃和0.01至10巴,其包括在存在下进行反应 的碱和季盐。