Process for hydroformylation of n-vinyl-2-pyrrolidinone
    132.
    发明授权
    Process for hydroformylation of n-vinyl-2-pyrrolidinone 失效
    N-乙烯基-2-吡咯烷酮加氢甲酰化方法

    公开(公告)号:US4831159A

    公开(公告)日:1989-05-16

    申请号:US876495

    申请日:1986-06-20

    Applicant: Jiang-Jen Lin

    Inventor: Jiang-Jen Lin

    CPC classification number: C07D207/27 C07C209/62 C07C213/00

    Abstract: A process is disclosed for preparing isomeric aldehydes by contacting N-vinyl-2-pyrrolidinone and synthesis gas in the presence of a rhodium-containing compound with or without additional phosphine ligand and a solvent. The alpha and beta isomeric aldehydes such as 2-N-(2-pyrrolionyl)propanaldehyde and 3-N-(2-pyrrolidonyl)propanaldehyde can be converted to 1,2- or 1,3-diaminopropanes via reductive amination or to alcohol amines via reduction.

    Abstract translation: 公开了通过在含或不含另外的膦配体和溶剂的含铑化合物的存在下使N-乙烯基-2-吡咯烷酮与合成气接触来制备异构醛的方法。 α和β异构醛如2-N-(2-吡咯啉基)丙醛和3-N-(2-吡咯烷酮基)丙醛可以通过还原胺化或醇胺转化为1,2-或1,3-二氨基丙烷 通过减少。

    Method for purification of amido acids
    134.
    发明授权
    Method for purification of amido acids 失效
    氨基酸纯化方法

    公开(公告)号:US4676933A

    公开(公告)日:1987-06-30

    申请号:US920826

    申请日:1986-10-20

    Applicant: Jiang-Jen Lin

    Inventor: Jiang-Jen Lin

    CPC classification number: C07C233/46

    Abstract: A method for purification of C.sub.12 -C.sub.16 amido acids prepared from C.sub.10 -C.sub.14 amido acids is disclosed. The amido acids are purificed by dissolving the crude product in organic alcohol solvent and chloroform at a temperature between room temperature and about 60.degree. C. and about atmospheric pressure. Then the solution is filtered, cooled and allowed to recrystallize. This method is effective for removing the Rh and Co bimetallic catalysts.

    Abstract translation: 公开了一种从C10-C14酰胺酸制备的C12-C16酰胺酸的纯化方法。 酰胺酸通过将粗产物溶解在有机醇溶剂和氯仿中,在室温至约60℃和约大气压之间的温度下进行纯化。 然后将溶液过滤,冷却并使其重结晶。 该方法对于去除Rh和Co双金属催化剂是有效的。

    Process for synthesis of ethylene glycol from synthesis gas plus
1,3-dioxolane using 1,3-dioxolane as a solvent
    135.
    发明授权
    Process for synthesis of ethylene glycol from synthesis gas plus 1,3-dioxolane using 1,3-dioxolane as a solvent 失效
    使用1,3-二氧戊环作为溶剂从合成气加上1,3-二氧戊环合成乙二醇的方法

    公开(公告)号:US4609768A

    公开(公告)日:1986-09-02

    申请号:US663602

    申请日:1984-10-22

    CPC classification number: C07C29/156

    Abstract: This invention relates to the manufacture of ethylene glycol and more particularly to a low pressure process for making ethylene glycol comprising reacting synthesis gas, i.e. a mixture of carbon monoxide and hydrogen, plus 1,3-dioxolane in the presence of a homogenous liquid catalyst containing an effective amount of cobalt-containing compound, a silane or germane-containing promoter dispersed in a dioxolane solvent at a temperature of at least 50.degree. C. and a pressure of at least 500 psi.

    Abstract translation: 本发明涉及乙二醇的制造,更具体地说,涉及用于制备乙二醇的低压方法,其包括使合成气(即一氧化碳和氢气的混合物)加上1,3-二氧戊环在含有 在至少50℃的温度和至少500psi的压力下分散在二氧戊环溶剂中的有效量的含钴化合物,含硅烷或含锗的促进剂。

    Preparation of enamines from conjugated dienes
    136.
    发明授权
    Preparation of enamines from conjugated dienes 失效
    从共轭二烯制备烯胺

    公开(公告)号:US4602088A

    公开(公告)日:1986-07-22

    申请号:US634925

    申请日:1984-07-26

    Applicant: Jiang-Jen Lin

    Inventor: Jiang-Jen Lin

    CPC classification number: C07D295/023 C07C209/60

    Abstract: A method for the preparation of enamines wherein a conjugated diene is reacted with a secondary amine, carbon monoxide and hydrogen (synthesis gas) in solvent solution in the presence of a rhodium catalyst. In accordance with the preferred embodiment, butadiene is reacted with a dialkylamine and synthesis gas in an organic solvent in the presence of a rhodium catalyst to provide the corresponding 1,3-pentadienyl dialkylamine in good yield and with good selectivity. This may be illustrated, for example, by the following equation: ##STR1##

    Abstract translation: 一种制备烯胺的方法,其中在铑催化剂存在下,在溶剂溶液中使共轭二烯与仲胺,一氧化碳和氢(合成气)反应。 根据优选实施方案,在铑催化剂的存在下,丁二烯与二烷基胺和合成气在有机溶剂中反应,以良好的收率和良好的选择性提供相应的1,3-戊二烯基二烷基胺。 这可以例如通过以下等式示出:图像H3CCHCHCHCHNR2 + H2O

    Process for oxidative dicarbonylation of butadiene
    138.
    发明授权
    Process for oxidative dicarbonylation of butadiene 失效
    丁二烯氧化二羰基化方法

    公开(公告)号:US4552976A

    公开(公告)日:1985-11-12

    申请号:US644470

    申请日:1984-08-27

    CPC classification number: C07C67/38

    Abstract: This invention relates to the carbonylation of olefins. More particularly it involves the carbonylation of aliphatic conjugated diolefins such as 1,3-butadiene to form adipic acid precursors such as, for example, dimethyl hex-3-ene-1,6-dioate by a process comprising reacting said 1,3-butadiene with carbon monoxide and oxygen in the presence of a hetergeneous palladium catalyst, a copper-containing compound and a lithium-containing compound.

    Abstract translation: 本发明涉及烯烃的羰基化。 更具体地涉及脂族共轭二烯烃例如1,3-丁二烯的羰基化以形成己二酸前体,例如己-3-烯-1,6-二酸二甲酯,其方法包括使所述1,3-丁二烯, 丁二烯与一氧化碳和氧气在异种钯催化剂,含铜化合物和含锂化合物存在下进行。

    Butadiene reductive dimerization using a platinum catalyst and polymeric
amine promoter
    139.
    发明授权
    Butadiene reductive dimerization using a platinum catalyst and polymeric amine promoter 失效
    使用铂催化剂和聚合胺助催化剂进行丁二烯还原二聚

    公开(公告)号:US4536604A

    公开(公告)日:1985-08-20

    申请号:US589805

    申请日:1984-03-15

    CPC classification number: C07C2/74 C07C2531/02 C07C2531/22

    Abstract: A method for preparing 1,6-octadiene by reacting 1,3-butadiene with formic acid in the presence of a platinum(II) catalyst and a polymeric tertiary amine catalyst is described. The combination of a platinum(II) catalyst such as platinum acetylacetonate with a polymeric tertiary amine promoter such as AMBERLYST.RTM. A21 macroreticular ion-exchange resin gives a high selectivity to 1,6-octadiene as opposed to the 1,7-octadiene form. A reaction temperature between 50.degree. and 150.degree. C. is preferred, and carbon dioxide and a solvent may also be employed.

    Abstract translation: 描述了在铂(II)催化剂和聚合叔胺催化剂存在下,使1,3-丁二烯与甲酸反应制备1,6-辛二烯的方法。 铂(II)催化剂如乙酰丙酮铂与聚合叔胺助催化剂如AMBERLYST TM A21大网络离子交换树脂的组合相对于1,7-辛二烯形式对1,6-辛二烯具有高选择性。 优选的反应温度为50-150℃,也可以使用二氧化碳和溶剂。

    Synthesis of substituted dioxolanes by direct oxidation of olefins over
molybdenum 8-hydroxyquinoline
    140.
    发明授权
    Synthesis of substituted dioxolanes by direct oxidation of olefins over molybdenum 8-hydroxyquinoline 失效
    通过在钼上羟基喹啉直接氧化烯烃来合成取代的二氧戊环

    公开(公告)号:US4526992A

    公开(公告)日:1985-07-02

    申请号:US662316

    申请日:1984-10-18

    CPC classification number: C07D215/30 C07D317/12 C07F11/005

    Abstract: The synthesis of substituted dioxolanes by direct oxidation of olefins over a molybdenum 8-hydroxyquinoline catalyst in the presence of water is described. An organic solvent such as chlorobenzene may also be employed. Water is essential to the reaction to make the dioxolanes, otherwise olefin oxides are produced. Hence, 4-methyl-1,3-dioxolane and 2,4-dimethyl-1,3-dioxolane were prepared from propylene oxidation, and three isomers of 2,4,5-trimethyl-1,3-dioxolane were prepared from 2-butene oxidation.

    Abstract translation: 描述了通过在水存在下在钼8-羟基喹啉催化剂上直接氧化烯烃的取代的二氧戊环的合成。 还可以使用有机溶剂如氯苯。 水是制备二氧戊环的反应所必需的,否则产生烯烃氧化物。 因此,由丙烯氧化制备4-甲基-1,3-二氧戊环和2,4-二甲基-1,3-二氧戊环,由2,5-二甲基-1,3-二氧戊环制备2,4,5-三甲基-1,3-二氧戊环的三种异构体 丁烯氧化。

Patent Agency Ranking