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    Method for preparing aromatic compounds
    2.
    发明授权
    Method for preparing aromatic compounds 失效
    芳香族化合物的制备方法

    公开(公告)号：US5886210A

    公开(公告)日：1999-03-23

    申请号：US876211

    申请日：1997-06-16

    申请人： Heather Lynnette Rayle ,  Randall Wayne Stephens

    发明人： Heather Lynnette Rayle ,  Randall Wayne Stephens

    IPC分类号： C07B61/00 ,  C07C45/65 ,  C07C51/377 ,  C07C67/317 ,  C07C231/12 ,  C07C253/30 ,  C07C69/76

    CPC分类号： C07C253/30 ,  C07B61/00 ,  C07C231/12 ,  C07C45/65 ,  C07C51/377 ,  C07C67/317

    摘要： A method for synthesizing aromatic compounds by selectively dehalogenating aromatic starting materials is provided. Compounds may be prepared which are substituted with fluoro, chloro or bromo. The method may be used to remove halogen atoms from sites at which halogenation is not desired, and to form substantially pure halogenated compounds from mixtures of starting materials. The method uses a copper containing dehalogenation agent and an acid with the dehalogenation being controlled by a substituent such as a carboxylic acid, amide, ester, aldehyde, ketone or cyano on the aromatic ring.

    摘要翻译： 提供了通过选择性脱卤芳族起始原料合成芳族化合物的方法。 可以制备被氟，氯或溴取代的化合物。 该方法可用于从不需要卤化的位置除去卤素原子，并从起始原料的混合物形成基本上纯的卤代化合物。 该方法使用含铜脱卤剂和在芳环上具有脱羧作用的酸由诸如羧酸，酰胺，酯，醛，酮或氰基之类的取代基控制。

    Process to chloroketones using oxazolines
    3.
    发明授权
    Process to chloroketones using oxazolines 失效
    使用恶唑啉的氯代酮的方法

    公开(公告)号：US5859254A

    公开(公告)日：1999-01-12

    申请号：US58832

    申请日：1998-04-13

    申请人： Heather Lynnette Rayle ,  Renee Caroline Roemmele ,  Randall Wayne Stephens

    发明人： Heather Lynnette Rayle ,  Renee Caroline Roemmele ,  Randall Wayne Stephens

    IPC分类号： B01J23/04 ,  C07B61/00 ,  C07C231/10 ,  C07C233/31 ,  C07C233/76 ,  C07D263/14 ,  C07D263/32 ,  C07D263/52 ,  C07D413/04 ,  C07D213/02 ,  C07C235/12

    CPC分类号： C07D263/52 ,  C07C231/10 ,  C07D263/14 ,  C07D263/32 ,  C07D413/04 ,  C07C2101/14

    摘要： This invention relates to a process for the preparation of an .alpha.-chloroketone compound comprising the steps of(i) cyclizing an alkynyl amide to form a 5-methyleneoxazoline ##STR1## (ii) chlorinating the 5-methyleneoxazoline using trichloroisocyanuric acid to produce a chlorinated oxazoline intermediate ##STR2## and (iii) hydrolyzing the chlorinated oxazoline intermediate with an aqueous acid to produce the desired monochloroketone ##STR3## wherein Z is alkyl or substituted alkyl, aryl or substituted aryl, heteroaryl or substituted heteroaryl or phenylene,R is a hydrogen atom or alkyl, andR.sup.1 and R.sup.2 are each independently an alkyl or substituted alkyl group, or R.sup.1 and R.sup.2 together with the carbon atom to which they are attached form a cyclic structure.Additionally, when R is a hydrogen atom, a dichloroketone can be conveniently formed through adjustment of reaction conditions.

    摘要翻译： 本发明涉及一种制备α-氯代酮化合物的方法，包括以下步骤：（i）使炔基酰胺环化以形成5-亚甲基恶唑啉（ii）使用三氯异氰脲酸氯化5-亚甲基恶唑啉以产生氯代 恶唑啉中间体+图像＆gt;和（iii）用含水酸水解氯代恶唑啉中间体以产生所需的单氯代酮其中Z是烷基或取代的烷基，芳基或取代的芳基，杂芳基或取代的杂芳基或亚苯基 R为氢原子或烷基，R 1和R 2各自独立地为烷基或取代的烷基，或者R 1和R 2与它们所连接的碳原子一起形成环状结构。 此外，当R是氢原子时，可以通过调整反应条件方便地形成二氯酮。

    Metal salt catalyzed process to oxazolines and subsequent formation of chloroketones
    4.
    发明授权
    Metal salt catalyzed process to oxazolines and subsequent formation of chloroketones 有权
    金属盐催化方法进行恶唑啉，随后形成氯代酮

    公开(公告)号：US6057477A

    公开(公告)日：2000-05-02

    申请号：US293119

    申请日：1999-04-16

    申请人： Heather Lynnette Rayle

    发明人： Heather Lynnette Rayle

    IPC分类号： B01J27/122 ,  B01J27/13 ,  B01J27/138 ,  B01J27/25 ,  B01J31/04 ,  C07B61/00 ,  C07C231/00 ,  C07C231/10 ,  C07C231/12 ,  C07C231/14 ,  C07C233/31 ,  C07C233/76 ,  C07D263/32 ,  C07C235/74 ,  C07C235/84

    CPC分类号： C07C231/12 ,  C07C231/10 ,  C07C231/14 ,  C07D263/32

    摘要： This invention relates to a process for the preparation of an .alpha.-chloroketone compound comprising the steps of(i) cyclizing an alkynyl amide to form a 5-methyleneoxazoline ##STR1## (ii) chlorinating the 5-methyleneoxazoline using trichlorolsocyanuric acid to produce a chlorinated oxazoline intermediate ##STR2## and (iii) hydrolyzing the chlorinated oxazoline intermediate with an aqueous acid to produce the desired monochloroketone ##STR3## wherein Z is alkyl or substituted alkyl, aryl or substituted aryl, heteroaryl or substituted heteroaryl or phenylene,R is a hydrogen atom or alkyl, andR.sup.1 and R.sup.2 are each independently an alkyl or substituted alkyl group, or R.sup.1 and R.sup.2 together with the carbon atom to which they are attached form a cyclic structure. Additionally, when R is a hydrogen atom, a dichloroketone can be conveniently formed through adjustment of reaction conditions.

    摘要翻译： 本发明涉及一种制备α-氯代酮化合物的方法，包括以下步骤：（i）使炔基酰胺环化以形成5-亚甲基恶唑啉（ii）使用三氯氰尿酸酸化5-亚甲基恶唑啉以产生氯化恶唑啉中间体， （iii）用含水酸水解氯代恶唑啉中间体以产生所需的一氯代酮，其中Z是烷基或取代的烷基，芳基或取代的芳基，杂芳基或取代的杂芳基或亚苯基，R是氢原子或烷基，R 1和R 2是 各自独立地是烷基或取代的烷基，或者R 1和R 2与它们所连接的碳原子一起形成环状结构。 此外，当R是氢原子时，可以通过调整反应条件方便地形成二氯酮。

    Process to chloroketones using oxazolines
    5.
    发明授权
    Process to chloroketones using oxazolines 失效
    使用恶唑啉的氯代酮的方法

    公开(公告)号：US5932738A

    公开(公告)日：1999-08-03

    申请号：US170642

    申请日：1998-10-13

    申请人： Heather Lynnette Rayle ,  Renee Caroline Roemmele ,  Randall Wayne Stephens

    发明人： Heather Lynnette Rayle ,  Renee Caroline Roemmele ,  Randall Wayne Stephens

    IPC分类号： B01J23/04 ,  C07B61/00 ,  C07C231/10 ,  C07C233/31 ,  C07C233/76 ,  C07D263/14 ,  C07D263/32 ,  C07D263/52 ,  C07D413/04

    CPC分类号： C07D263/52 ,  C07C231/10 ,  C07D263/14 ,  C07D263/32 ,  C07D413/04 ,  C07C2101/14

    摘要： This invention relates to a process for the preparation of an .alpha.-chloroketone compound comprising the steps of(i) cyclizing an alkynyl amide to form a 5-methyleneoxazoline ##STR1## (ii) chlorinating the 5-methyleneoxazoline using trichloroisocyanuric acid to produce a chlorinated oxazoline intermediate ##STR2## and (iii) hydrolyzing the chlorinated oxazoline intermediate with an aqueous acid to produce the desired monochloroketone ##STR3## wherein Z is alkyl or substituted alkyl, aryl or substituted aryl, heteroaryl or substituted heteroaryl or phenylene,R is a hydrogen atom or alkyl andR.sup.1 and R.sup.2 are each independently an alkyl or substituted alkyl group, or R.sup.1 and R.sup.2 together with the carbon atom to which they are attached form a cyclic structure.Additionally, when R is a hydrogen atom, a dichloroketone can be conveniently formed through adjustment of reaction conditions.

    摘要翻译： 本发明涉及一种制备α-氯代酮化合物的方法，其包括以下步骤：（i）使炔基酰胺环化以形成5-亚甲基恶唑啉（ii）使用三氯异氰脲酸氯化5-亚甲基恶唑啉以产生氯化恶唑啉中间体， （iii）用含水酸水解氯代恶唑啉中间体以产生所需的一氯代酮，其中Z是烷基或取代的烷基，芳基或取代的芳基，杂芳基或取代的杂芳基或亚苯基，R是氢原子或烷基，R 1和R 2各自 独立地是烷基或取代的烷基，或者R 1和R 2与它们所连接的碳原子一起形成环状结构。 此外，当R是氢原子时，可以通过调整反应条件方便地形成二氯酮。

    Process to chloroketones using oxazolines
    7.
    发明授权
    Process to chloroketones using oxazolines 失效
    使用恶唑啉的氯代酮的方法

    公开(公告)号：US5925763A

    公开(公告)日：1999-07-20

    申请号：US170344

    申请日：1998-10-13

    申请人： Heather Lynnette Rayle ,  Renee Caroline Roemmele ,  Randall Wayne Stephens

    发明人： Heather Lynnette Rayle ,  Renee Caroline Roemmele ,  Randall Wayne Stephens

    IPC分类号： B01J23/04 ,  C07B61/00 ,  C07C231/10 ,  C07C233/31 ,  C07C233/76 ,  C07D263/14 ,  C07D263/32 ,  C07D263/52 ,  C07D413/04 ,  C07D213/02 ,  C07C233/01 ,  C07C233/11

    CPC分类号： C07D263/52 ,  C07C231/10 ,  C07D263/14 ,  C07D263/32 ,  C07D413/04 ,  C07C2101/14

    摘要： This invention relates to a process for the preparation of an .alpha.-chloroketone compound comprising the steps of(i) cyclizing an alkynyl amide to form a 5-methyleneoxazoline ##STR1## (ii) chlorinating the 5-methyleneoxazoline using trichloroisocyanuric acid to produce a chlorinated oxazoline intermediate ##STR2## and (iii) hydrolyzing the chlorinated oxazoline intermediate with an aqueous acid top produce the desired monochloroketone ##STR3## wherein Z is alkyl or substituted alkyl, aryl or substituted aryl, heteroaryl or substituted heteroaryl or phenylene,R is a hydrogen atom or alkyl, andR.sup.1 and R.sup.2 are each independently an alkyl or substituted alkyl group, or R.sup.1 and R.sup.2 together with the carbon atom to which they are attached form a cyclic structure.Additionally, when R is a hydrogen atom, a dichioroketone can be conveniently formed through adjustment of reaction conditions.

    摘要翻译： 本发明涉及一种制备α-氯代酮化合物的方法，其包括以下步骤：（i）使炔基酰胺环化以形成5-亚甲基恶唑啉（ii）使用三氯异氰脲酸氯化5-亚甲基恶唑啉以产生氯化恶唑啉中间体， （iii）用酸水溶液水解氯代恶唑啉中间体产生所需的单氯代酮，其中Z是烷基或取代的烷基，芳基或取代的芳基，杂芳基或取代的杂芳基或亚苯基，R是氢原子或烷基，R1和R2是 各自独立地是烷基或取代的烷基，或者R 1和R 2与它们所连接的碳原子一起形成环状结构。 此外，当R为氢原子时，通过调整反应条件可以方便地形成二酮酮。