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    • 3. 发明授权
    • Process for preparing phenylacetic acid derivatives
    • 制备苯乙酸衍生物的方法
    • US06653502B2
    • 2003-11-25
    • US10037078
    • 2001-11-09
    • Holger Geissler
    • Holger Geissler
    • C07C6736
    • C07C51/10C07C67/36C07C57/32C07C57/58C07C69/612
    • A process for preparing phenylacetic acid derivatives of the formula (I) by reacting benzyl chlorides of the formula (II) with a compound of the formula R6OH and with carbon monoxide in a dipolar aprotic solvent in the presence of a catalyst which comprises at least one compound of a transition metal of subgroup VIII of the Periodic Table of the Elements, where R1, R2, R3, R4, and R5 independently of one another are the following radicals: a hydrogen or fluorine atom; a CH2Cl radical; a HO2CCH═CH—, NC— or CF3— group; an alkyl, alkoxy or acyloxy radical having in each case 1 to 18 carbon atoms; or a C6-C18-aryloxy, aryl or heteroaryl radical.
    • 一种制备式(I)的苯乙酸衍生物的方法,其通过式(II)的苄基氯与式R 6 OH的化合物和一氧化碳在偶极非质子传递溶剂中在催化剂存在下反应, 包括至少一种元素周期表第VIII族过渡金属的化合物,其中R 1,R 2,R 3,R 4和R 5彼此独立地是 是以下基团:氢或氟原子; CH 2 Cl基; HO 2 CCH = CH-,NC-或CF 3 - 基团;在每种情况下具有1至18个碳原子的烷基,烷氧基或酰氧基; 或C 6 -C 18芳氧基,芳基或杂芳基。
    • 4. 发明授权
    • Method for the catalytic production of substituted bipyridyl derivatives
    • 催化生产取代联吡啶衍生物的方法
    • US06500956B1
    • 2002-12-31
    • US09674063
    • 2000-11-30
    • Holger GeisslerPeter Gross
    • Holger GeisslerPeter Gross
    • C07D40102
    • C07B37/04C07D213/22C07D213/64C07D213/803
    • The invention relates to a process for the preparation of bipyridyls by converting at least one pyridine of the formula (III) in which S′, S″, S′″, S″″ and S′″″, independently of one another, are identical or different and are hydrogen, (C1-C18)-alkyl, alkoxy-(C1-C18), acyloxy-(C1-C18), aryloxy-(C1-C18), perfluoroacyloxy-(C1-C8), NO2, (C1-C18)-aryl, (C1-C18)-heteroaryl, halogen, hydroxyl, nitro, nitroso, CN, COOH, CHO, PO3H2, SO3H, SO2R, SOR, NH2, NH-alkyl-(C1-C18), N-alkyl2-(C1-C18), protected amine, CF3, NHCO-alkyl-(C1-C4), N-alkyl-(C1-C4)-CO-alkyl-(C1-C4), COO-alkyl-(C1-C18), CONH2, CO-alkyl-(C1-C18), NHCOH, NHCOO-alkyl-(C1-C4), CO-(C1-C18)-aryl, COO-(C1-C18)-aryl, CHCH-CO2-alkyl-(C1-C18), CHCHCO2H, PO-phenyl2, PO-alkyl2-(C1-C4), (COO−)n(cation)n+, (PO32−)n(cation)2n+, (SO3−)n(cation)n+ and/or (O−)n(cation)n+, where optionally S′, S″, S′″, S″″ and/or S′″″ among one another together form one or more aliphatic and/or aromatic rings and/or in which optionally S′, S″, S′″, S″″and/or S′″″forms a bridge to at least one further pyridine of the formula (III) and/or in which optionally the radicals S′, S″, S′″, S″″, and/or S′″″ have the meanings given above and are substituted by at least one radical which has the meaning given above for S′, S″, S′″, S″″ and/or S′″″ in water in the presence of an alcohol, a base, a palladium catalyst and optionally one or more further solvents at a temperature of 0-200° C.
    • 本发明涉及通过将至少一种式(III)的吡啶独立地转化成其中S',S“,S”',S“”和“”“的吡啶来制备联吡啶的方法。 (C 1 -C 18),酰氧基 - (C 1 -C 18),芳氧基 - (C 1 -C 18),全氟酰氧基 - (C 1 -C 8)烷基, ),NO2,(C1-C18) - 芳基,(C1-C18) - 杂芳基,卤素,羟基,硝基,亚硝基,CN,COOH,CHO,PO3H2,SO3H,SO2R,SOR,NH2,NH-烷基 - (C1 (C1-C4)-CO-烷基 - (C1-C4),CO-烷基 - (C1-C4)-CO-烷基 - (C1-C4) (C 1 -C 18) - 烷基 - (C 1 -C 18),CONH 2,CO-烷基 - (C 1 -C 18),NHCOH,NHCOO-烷基 - (C 1 -C 4) 芳基,CHCH-CO 2 - 烷基 - (C 1 -C 18),CHCHCO 2 H,PO-苯基2,PO-烷基2-(C 1 -C 4),(COO-)n(阳离子)n +,(PO32-) ,(SO 3 - )n(阳离子)n +和/或(O-)n(阳离子)n +,其中任选地有S',S“,S”',S“'和/或S” “彼此在一起形成一个或多个脂族和/或芳香环和/或其中任选的S',S”,S“',S” '和/或S''''与至少一种式(III)的另外的吡啶形成桥,和/或其中任选的基团S',S“,S”',S“ '和/或S'''具有上述含义,并被至少一个具有上述意义的基团代替S',S“,S”,S“”和/ 在醇,碱,钯催化剂和任选的一种或多种其它溶剂的存在下,在0-200℃的温度下,在水中加入S“或”S“
    • 5. 发明授权
    • Process for preparing isochroman-3-ones
    • 异苯并二氢吡喃-3-酮的制备方法
    • US6075152A
    • 2000-06-13
    • US286566
    • 1999-04-05
    • Holger GeisslerRalf Pfirmann
    • Holger GeisslerRalf Pfirmann
    • B01J31/24C07B61/00C07D311/76C07D311/74
    • C07D311/76
    • The present invention relates to a process for preparing an isochroman-3-one of the formula (I) by reacting a 1,2-bishalomethylbenzene of the formula (II) ##STR1## in which X is chlorine, bromine or iodine with carbon monoxide and water at a CO pressure of from 0.1 to 50 MPa and a temperature of from 20 to 200.degree. C. in the presence or absence of an ionic halide, in the presence of a palladium catalyst and a dipolar aprotic solvent, where in the formulae (I) and (II) the radicals R.sup.1, R.sup.2, R.sup.3 and R.sup.4 independently of one another denote:a hydrogen or fluorine atom;a HO.sub.2 CCH.dbd.CH--, NC-- or F.sub.3 C group;an alkyl, alkoxy or acyloxy radical having in each case 1 to 18 carbon atoms; or a C.sub.6 -C.sub.18 -aryloxy, aryl or heteroaryl radical, where the heteroatoms present are 1 to 3 atoms from the group O, N and/or S;a R.sup.5.sub.2 P(.dbd.O)--, R.sup.6 C(.dbd.O)--, R.sup.6 OC(.dbd.O)--, R.sup.6 OC(.dbd.O)CH.dbd.CH--, R.sup.7 C(.dbd.O)--, R.sup.7 OC(.dbd.O)CH.dbd.CH-- or R.sup.7.sub.2 P(.dbd.O) radical; in which R.sup.5 is a C.sub.1 -C.sub.4 -alkyl radical, R.sup.6 is a C.sub.1 -C.sub.18 -alkyl radical and R.sup.7 is a C.sub.6 -C.sub.18 -aryl radical; or in which at least one of the radicals R.sup.1, R.sup.2, R.sup.3 and R.sup.4 is substituted by a radical R.sup.8, where R.sup.8 has the same meaning as R.sup.1 ; or where at least two of the radicals R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are linked with one another and form at least one aliphatic or aromatic ring having 5 to 18 carbon atoms.
    • 本发明涉及通过使式(II)的1,2-二沙甲基苯(其中X为氯,溴或碘)与一氧化碳和水反应制备式(I)的异苯并二氢吡喃-3-酮的方法, 在钯催化剂和偶极非质子传递溶剂存在下,在离子型卤化物存在或不存在下,在0.1至50MPa的CO压力和20至200℃的温度下,其中式(I) 和(II)基团R 1,R 2,R 3和R 4彼此独立地表示:氢或氟原子; HO2CCH = CH-,NC-或F3C组; 在每种情况下具有1至18个碳原子的烷基,烷氧基或酰氧基; 或C 6 -C 18芳氧基,芳基或杂芳基,其中存在的杂原子是基团O,N和/或S 1至3个原子; (= O) - ,R6C(= O) - ,R6OC(= O) - ,R6OC(= O)CH = CH-,R7C(= O) - ,R7OC(= O)CH = CH-或R72P (= O)基团; 其中R 5是C 1 -C 4 - 烷基,R 6是C 1 -C 18烷基,R 7是C 6 -C 18芳基; 或其中基团R 1,R 2,R 3和R 4中的至少一个被基团R 8取代,其中R 8具有与R 1相同的含义; 或者其中基团R 1,R 2,R 3和R 4中的至少两个彼此连接并形成至少一个具有5至18个碳原子的脂族或芳族环。
    • 7. 发明授权
    • Process for the preparation of 3-isochromanoes by cyclization of o-chloromethylphenylacetic acids
    • 通过邻氯甲基苯基乙酸的环化制备3-异色烯的方法
    • US06215006B1
    • 2001-04-10
    • US09574332
    • 2000-05-19
    • Holger Geissler
    • Holger Geissler
    • C07D31174
    • C07D311/76
    • The present invention relates to a process for the preparation of a 3-isochromanone of the formula (I) by reaction of an o-chloromethylphenylacetic acid of the formula (II) at a temperature of 100 to 250° C. in the presence or absence of an ionic halide, in the presence or absence of an organic solvent with and removal of hydrogen chloride, where in the formulae (I) and (II) the radicals R1, R2, R3 and R4 independently of one another are: a hydrogen or fluorine atom; an NC or F3C group; an alkyl alkoxy or acyloxy radical, each having 1 to 18 carbon atoms; or a C6-C18-aryloxy, aryl or heteroaryl radical, 1 to 3 atoms from the group consisting of O, N and/or S being present as heteroatoms; or in which at least two of the radicals R1, R2, R3 and R4 are linked to one another and form at least one aliphatic or aromatic ring having 5 to 18 carbon atoms.
    • 本发明涉及通过式(II)的邻氯甲基苯基乙酸在100-250℃的温度下,在存在或不存在下反应制备式(I)的3-异色满酮的方法 在存在或不存在有机溶剂和除去氯化氢的情况下,离子卤化物,其中在式(I)和(II)中,基团R 1,R 2,R 3和R 4彼此独立地是:氢或 氟原子; NC或F3C基团;烷基烷氧基或酰氧基,各自具有1至18个碳原子; 或C 1 -C 18芳氧基,芳基或杂芳基,其中1至3个原子来自O,N和/或S作为杂原子存在;或其中R1,R2,R3和R4中的至少两个 彼此连接并形成至少一个具有5至18个碳原子的脂族或芳族环。
    • 8. 发明授权
    • Dipalladaphosphacyclobutanes and a process for preparing the same
    • 二环磷杂环丁烷及其制备方法
    • US6084114A
    • 2000-07-04
    • US308259
    • 1999-07-19
    • Holger GeisslerPeter GrossBianca Guckes
    • Holger GeisslerPeter GrossBianca Guckes
    • B01J31/24C07F15/00C07F9/02
    • B01J31/2404B01J31/24B01J31/2423B01J31/2447C07F15/006B01J2231/4261B01J2531/0205B01J2531/824B01J2540/225
    • The invention relates to palladaphosphacyclobutanes of the formula (I) ##STR1## where R.sup.1, R.sup.2 are, independently of one another, hydrogen, (C.sub.1 -C.sub.4)-alkyl, (C.sub.3 -C.sub.12)-cycloalkyl, (C.sub.1 -C.sub.4)-alkoxy, fluorine, N[(C.sub.1 -C.sub.4)-alkyl].sub.2, CO.sub.2 -(C.sub.1 -C.sub.4)-alkyl, OCO-(C.sub.1 -C.sub.4)-alkyl or aryl;R.sup.3, R.sup.4, R.sup.5, R.sup.6 are, independently of one another, (C.sub.1 -C.sub.8)-alkyl, (C.sub.3 -C.sub.12)-cycloalkyl or aryl;or where R.sup.1 and R.sup.2, R.sup.1 or R.sup.2 and R.sup.3 or R.sup.4, R.sup.3 and R.sup.4, R.sup.3 or R.sup.4 and R.sup.5 or R.sup.6, or R.sup.5 and R.sup.6 together form an aliphatic ring; or where R.sup.5 and R.sup.6, R.sup.3 or R.sup.4 and R.sup.5 or R.sup.6 together form an aromatic ring; andY is an anion of an inorganic or organic acid, with the exception of the compoundsdi-.mu.-chloro-bis[2-[bis(1,1-dimethylethyl)phosphino]-2-methylpropyl-C,P]dipalladium(II)di-.mu.-bromo-bis[2-[bis(1,1 -dimethylethyl)phosphino]-2-methylpropyl-C,P]dipalladium(II)di-.mu.-trifluoroacetato-bis[2-[bis(1,1 -dimethylethyl)phosphino]-2-methylpropyl-C,P]dipalladium(II)di-.mu.-chloro-bis[2-[(1,1 -dimethylethyl)phenylphosphino]-2-methylpropyl-C,P]dipalladium(II).mu.-chloro-.mu.-methoxy-bis[2-[bis(1,1 -dimethylethyl)phosphino]-2-methylpropyl-C,P]dipalladium(II).
    • PCT No.PCT / EP97 / 06327 Sec。 371日期1999年7月19日第 102(e)1999年7月19日PCT 1997年11月13日PCT公布。 公开号WO98 / 22485 日本公开日1998年5月28日本发明涉及式(I)的聚苯撑磷杂环丁烷,其中R1,R2彼此独立地为氢,(C1-C4) - 烷基,(C3-C12) - 环烷基,(C1-C4) - 烷氧基,氟,N [(C 1 -C 4) - 烷基] 2,CO 2 - (C 1 -C 4) - 烷基,OCO-(C 1 -C 4) - 烷基或芳基; R3,R4,R5,R6彼此独立地为(C1-C8) - 烷基,(C3-C12) - 环烷基或芳基; 或其中R 1和R 2,R 1或R 2和R 3或R 4,R 3和R 4,R 3或R 4和R 5或R 6或R 5和R 6一起形成脂族环; 或其中R 5和R 6,R 3或R 4和R 5或R 6一起形成芳环; 并且Y是无机或有机酸的阴离子,除了化合物二氯 - 双[2- [二(1,1-二甲基乙基)膦基] -2-甲基丙基-C,P]二钯( II)二 - 双 - 双 - [2- [二(1,1-二甲基乙基)膦基] -2-甲基丙基-C,P]二 - (三氟乙酰)双[ ,1-二甲基乙基)膦基] -2-甲基丙基-C,P]二钯(II)二氯 - 双[2 - [(1,1-二甲基乙基)苯基膦基] -2-甲基丙基C,P]二钯 (II) - 氯 - 甲氧基 - 双[2- [二(1,1-二甲基乙基)膦基] -2-甲基丙基-C,P]二钯(II)。