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Catalytic ionic hydrogenation of ketones using tungsten or molybdenum organometallic species

机译:使用钨或钼有机金属物质催化酮进行离子加氢

摘要

The present invention is a process for the catalytic hydrogenation of ketones and aldehydes to alcohols at low temperatures and pressures using organometallic molybdenum and tungsten complexes. The functional group is selected from groups represented by the formulas R(C═O)R' and R(C═ O)H, wherein R and R' are selected from hydrogen or any alkyl or aryl group. The active catalyst for the process has the form: [CpM(CO).sub.2 (PR*.sub.3) L].sup.+ A.sup.-, where Cp=&eegr; .sup.5 -R.sup. .tangle- solidup..sub.m C.sub.5 H.sub.5-m and R.sup.▴ represents an alkyl group or a halogen (F, Cl, Br, I) or R.sup..tangle- solidup. =OR' (where R'=H, an alkyl group or an aryl group) or R.sup.. tangle-solidup. =CO.sub.2 R' (where R'=H, an alkyl group or an aryl group) and m=0 to 5; M represents a molybdenum atom or a tungsten atom; R*.sub. 3 represents three hydrocarbon groups selected from a cyclohexyl group (C. sub.6 H.sub. 11), a methyl group (CH.sub.3), and a phenyl group (C.sub.6 H.sub.5) and all three R* groups can be the same or different or two of the three groups can be the same; L represents a ligand; and A. sup.- represents an anion. In another embodiment, one, two or three of the R* groups can be an OR*.
机译:本发明是使用有机金属钼和钨配合物在低温和低压下将酮和醛催化氢化为醇的方法。官能团选自由式R(C═ O)R'和R(C═ O)H表示的基团,其中R和R'选自氢或任何烷基或芳基。该方法的活性催化剂具有以下形式:[CpM(CO)2(PR * 3)L] + A--,其中Cp =&eegr; .sup.5 -R.sup。 Tangle-solidup.sub.m.C.sub.5 H.sub.5-m和R.sup。▴代表烷基或卤素(F,Cl,Br,I)或R.固结。 = OR′(其中R′= H,烷基或芳基)或R ..缠结固结。 = CO 2 R′(其中R′= H,烷基或芳基),m = 0-5。 M表示钼原子或钨原子; R * .sub。 3表示选自环己基(C.sub.6 H.sub.11),甲基(CH.sub.3)和苯基(C.sub.6 H.sub.5)的三个烃基三个R *基团可以相同或不同,或者三个基团中的两个可以相同; L代表配体; A. sup。-代表阴离子。在另一个实施方案中,R *基团中的一个,两个或三个可以是OR *。

著录项

  • 公开/公告号US6124509A

    专利类型

  • 公开/公告日2000-09-26

    原文格式PDF

  • 申请/专利权人 BROOKHAVEN SCIENCE ASSOCIATES;

    申请/专利号US19990235207

  • 发明设计人 R. MORRIS BULLOCK;MARK VOGES;

    申请日1999-01-22

  • 分类号C07C29/14;

  • 国家 US

  • 入库时间 2022-08-22 01:36:07

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