Preparation of 5-methylbutyrolactone
    1.
    发明授权
    Preparation of 5-methylbutyrolactone 失效
    5-甲基丁酰胺的制备

    公开(公告)号:US5189182A

    公开(公告)日:1993-02-23

    申请号:US236199

    申请日:1988-08-25

    IPC分类号: C07D315/00

    CPC分类号: C07D315/00

    摘要: 5-Methylbutyrolactone is prepared by a process in which a pentenoic ester of the formula IX--CO.sub.2 R (I),where X is CH.sub.2 .dbd.CH--CH.sub.2 --CH.sub.2 --, CH.sub.3 --CH.dbd.CH--CH.sub.2 -- or CH.sub.3 --CH.sub.2 --CH.dbd.CH-- and R is alkyl, cycloalkyl, aralkyl or aryl, or a mixture of these esters is reacted with water at from 50.degree. to 350.degree. C. in the presence or absence of a diluenta) over a zeolite and/or phosphate catalyst orb) in the presence of from 0.01 to 0.25 mole of a sulfonic acid, a Lewis acid and/or a non-oxidizing mineral acid per mole of pentenoic ester or over from 0.1 to 40% by weight, based on the pentenoic ester, of a strongly acidic ion exchanger as a catalyst in a first stage, or the pentenoic ester of the formula I, where X and R have the stated meanings, is hydrolyzed in a first stage with the aid of a strongly acidic ion exchanger as a catalyst to give the pentenoic acid of the formula I, where R is hydrogen, and the resulting pentenoic acid is subjected to cyclization in a second stage in the presence of from 0.005 to 0.1 mole of a sulfonic acid, a Lewis acid or a non-oxidizing mineral acid per mole of pentenoic acid or over from 0.1 to 20% by weight, based on the pentenoic acid, of a strongly acidic ion exchanger at from 50.degree. to 350.degree. C.

    摘要翻译: 通过以下方法制备5-甲基丁内酯,其中式I X-CO 2 R(I)的戊烯酸酯,其中X为CH 2 = CH-CH 2 -CH 2 - ,CH 3 -CH = CH-CH 2 - 或CH 3 -CH 2 -CH = CH-和R是烷基,环烷基,芳烷基或芳基,或这些酯的混合物与水在50-350℃下在存在或不存在稀释剂a)的情况下与沸石和/或磷酸盐 催化剂或b)在0.01至0.25摩尔磺酸,路易斯酸和/或非氧化性无机酸/摩尔烯酸酯存在下或基于戊烯酸酯为0.1至40重量% 的作为第一阶段的催化剂的强酸性离子交换剂或其中X和R具有所述含义的式I的戊烯酸在第一阶段中借助于强酸性离子交换剂作为 催化剂得到式I的戊烯酸,其中R是氢,所得戊烯酸在第二阶段中在0.005t的存在下进行环化 o 0.1摩尔磺酸,路易斯酸或非氧化性无机酸/摩尔烯酸,或超过0.1-20重量%,基于戊烯酸,强酸性离子交换剂为50〜 350℃

    Preparation of alkenecarboxylic esters
    3.
    发明授权
    Preparation of alkenecarboxylic esters 失效
    烷基羧酸酯的制备

    公开(公告)号:US5144061A

    公开(公告)日:1992-09-01

    申请号:US116865

    申请日:1987-11-05

    CPC分类号: C07C67/03

    摘要: The present invention relates to a method for producing optically active alcohol derivatives, which are useful as fungicides, herbicides or plant growth regulators, represented by the formula, ##STR1## by carrying out the asymmetric reduction of a ketone compound represented by the formula, ##STR2## with a boron hydride-reducing agent modified with an optically active amino alcohol represented by the formula, ##STR3## and also relates to the boron hydride type compound obtained by reacting the above optically active amino alcohol with a boron hydride compound and its production method.

    摘要翻译: 本发明涉及一种光学活性醇衍生物的制备方法,其可用作杀真菌剂,除草剂或植物生长调节剂,由下式表示:通过进行由式表示的酮化合物的不对称还原, IMAGE>与用式表示的光学活性氨基醇改性的硼氢化物还原剂,也涉及通过使上述光学活性氨基醇与硼氢化合物反应获得的硼氢化物型化合物及其生产 方法。

    Preparation of tetrahydrofurans from butane-1,4-diols
    5.
    发明授权
    Preparation of tetrahydrofurans from butane-1,4-diols 失效
    从丁烷-1,4-二醇制备四氢呋喃

    公开(公告)号:US4904806A

    公开(公告)日:1990-02-27

    申请号:US251391

    申请日:1988-09-30

    IPC分类号: C07D307/06

    CPC分类号: C07D307/06

    摘要: Tetrahydrofurans are prepared in the gas phase from butane-1,4-diols which may be substituted by alkyl, alkenyl and/or aryl radicals in the carbon skeleton. The reaction is carried out in the presence of a borosilicate and/or iron silicate zeolite, preferably of the pentasil type, as catalyst.Other catalysts which may be used are zeolites doped with alkali metals and/or alkaline earth metals and/or transition metals and/or rare earth metals and/or noble metals.

    摘要翻译: 四氢呋喃在气相中由丁烷-1,4-二醇制备,其可以在碳骨架中被烷基,烯基和/或芳基取代。 该反应在硼硅酸盐和/或铁硅酸盐沸石(优选pentasil型)作为催化剂的存在下进行。 可以使用的其它催化剂是掺杂有碱金属和/或碱土金属和/或过渡金属和/或稀土金属和/或贵金属的沸石。

    Preparation of cyclopentanone
    6.
    发明授权
    Preparation of cyclopentanone 失效
    环戊酮的制备

    公开(公告)号:US4822920A

    公开(公告)日:1989-04-18

    申请号:US116879

    申请日:1987-11-05

    IPC分类号: B01J29/04 B01J29/40 C07C45/48

    CPC分类号: B01J29/40 B01J29/04 C07C45/48

    摘要: Cyclopentanone is prepared from adipic esters by reacting adipic esters of the formulaR.sup.1 OOC--(CH.sub.2).sub.4 --COOR.sup.2where R.sup.1 and R.sup.2 are alkyl of 1 to 12 carbon atoms, cycloalkyl of 5 or 6 carbon atoms, aralkyl or aryl and R.sup.2 can additionally be hydrogen, in the gas or liquid phase at from 150.degree. C. to 450.degree. C. in the presence of zeolitic catalysts and/or phosphate catalysts, preferably zeolites of the pentasil type.

    摘要翻译: 环己酮由己二酸酯通过使式R1OOC-(CH2)4-COOR2的己二酸酯反应制备,其中R 1和R 2是1至12个碳原子的烷基,5或6个碳原子的环烷基,芳烷基或芳基, 氢气,在沸石催化剂和/或磷酸盐催化剂存在下,在150℃至450℃的气相或液相中,优选为pentasil型沸石。

    Preparation of organophosphorus compounds
    8.
    发明授权
    Preparation of organophosphorus compounds 失效
    有机磷化合物的制备

    公开(公告)号:US4922025A

    公开(公告)日:1990-05-01

    申请号:US216612

    申请日:1988-07-08

    IPC分类号: C07F9/50

    CPC分类号: C07F9/5059 Y02P20/582

    摘要: Organophosphorus compounds are prepared by reacting an unsaturated compound, such as a striaght-chain, branched or cyclic olefin or a diene having conjugated or nonconjugated double bonds, with a phosphine by a process in which phosphine and/or phosphine-containing compounds are subjected to an addition reaction with the unsaturated compounds in the presence of a solid heterogeneous catalyst. Particularly suitable heterogeneous catalysts are zeolites and phosphates.

    摘要翻译: 有机磷化合物通过使不饱和化合物,如条纹链,支链或环状烯烃或具有共轭或非共轭双键的二烯与膦合成,其中膦和/或含膦化合物经受 在固体多相催化剂存在下与不饱和化合物的加成反应。 特别合适的非均相催化剂是沸石和磷酸盐。