Preparation of 2,2-disubstituted 3-chloropropionic esters
    41.
    发明授权
    Preparation of 2,2-disubstituted 3-chloropropionic esters 失效
    2,2-二取代的3-氯丙酸酯的制备

    公开(公告)号:US4837357A

    公开(公告)日:1989-06-06

    申请号:US111624

    申请日:1987-10-21

    CPC classification number: C07C67/307 C07C67/03 C07C67/44

    Abstract: 2,2-Disubstituted 3-chloropropionic esters I ##STR1## where R.sup.1 and R.sup.2 are each C.sub.1 -C.sub.6 -alkyl, C.sub.2 -C.sub.6 -oxaalkyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -oxaalkenyl, aryl or C.sub.7 -C.sub.12 -aralkyl or R.sup.1 -C-R.sup.2 is 5-, 6- or 7-membered ring, R.sup.3 is C.sub.2 -C.sub.6 -oxaalkyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -oxaalkenyl or C.sub.7 -C.sub.12 -aralkyl, are prepared by converting 2,2-disubstituted 3-hydroxypropanals II ##STR2## into the esterdiol III ##STR3## reacting this esterdiol III in the presence of a transesterification catalyst with an alcohol R.sup.3 OH to give the 3-hydroxyester IV ##STR4## reacting the hydroxyester IV with a stoichiometric or greater than stoichiometric amount of the thionyl chloride and thermally decomposing the product to give the chloropropionic ester I.

    Abstract translation: 2,2-二取代的3-氯丙酸酯I,其中R 1和R 2各自是C 1 -C 6 - 烷基,C 2 -C 6 - 氧杂烷基,C 2 -C 6 - 烯基,C 2 -C 6 - 氧杂链烯基,芳基或C 7 -C 12 - 芳烷基或R1-C-R2是5-,6-或7-元环,R3是C2-C6-氧杂烷基,C2-C6-烯基,C2-C6-氧杂链烯基或C7-C12-芳烷基,是通过将2 将2-二取代的3-羟基丙醛II转化成酯二醇III在酯交换催化剂与醇R 3 OH的存在下使该酯二醇III反应,得到3-羟基酯IV使羟基酯IV 化学计量或大于化学计量的亚硫酰氯,并热分解产物得到氯丙酸酯I.

    Method of preparation of novel
2-(alkoxymethyl)-pentane-1,5-diisocyanates,
2-(alkoxymethyl)-pentane-1,5-diurethanes, and
2-(alkoxymethyl)-pentane-1,5-dicarbamic acid chlorides and their uses
    42.
    发明授权
    Method of preparation of novel 2-(alkoxymethyl)-pentane-1,5-diisocyanates, 2-(alkoxymethyl)-pentane-1,5-diurethanes, and 2-(alkoxymethyl)-pentane-1,5-dicarbamic acid chlorides and their uses 失效
    2-(烷氧基甲基) - 戊烷-1,5-二异氰酸酯,2-(烷氧基甲基) - 戊烷-1,5-二氨基甲酸酯和2-(烷氧基甲基) - 戊烷-1,5-二氨基酰氯的制备方法和 他们的用途

    公开(公告)号:US4748226A

    公开(公告)日:1988-05-31

    申请号:US97505

    申请日:1987-09-16

    Abstract: This invention relates to novel 2-(alkoxymethyl) pentane-1,5-diisocyanates, 2-(alkoxymethyl)-pentane-1,5-diurethanes, and 2-(alkoxymethyl)-pentane 1,5-dicarbamic acid chlorides having the structure: ##STR1## in which R is a straight chain or branched C.sub.1 -C.sub.20 -alkyl radical, a straight chain or branched C.sub.2 -C.sub.20 -alkenyl radical, a straight chain or branched C.sub.3 -C.sub.20 -oxaalkyl radical, an optionally substituted C.sub.5 -C.sub.12 -cycloalkyl radical, or an optionally substituted C.sub.7 -C.sub.20 -aralkyl radical and X is a --NCO--, --NH--CO.sub.2 R.sup.1 --, --NHCO.sub.2 R.sup.2 -- OR - NHCOCl-group whereby R.sup.1 and R.sup.2 can be the same or different and are a straight chain or branched C.sub.1 -C.sub.20 -alkyl radical or a C.sub.5 -C.sub.12 cycloalkyl radical, as well as a process for their preparation. The 2-(alkoxymethyl)-pentane-1,5-diurethanes or 2- (alkoxymethyl)-pentane-1,5-dicarbamic acid chlorides are suited for the preparation of 2-(alkoxymethyl)-pentane-1,5-diisocyanates, which in turn are used for the preparation of plastics using the polyisocyanate addition polymerization process.

    Abstract translation: 本发明涉及新型2-(烷氧基甲基)戊烷-1,5-二异氰酸酯,2-(烷氧基甲基) - 戊烷-1,5-二氨基甲酸酯和2-(烷氧基甲基) - 戊烷1,5-二氨基甲酰氯, :其中R是直链或支链C 1 -C 20烷基,直链或支链C 2 -C 20 - 烯基,直链或支链C 3 -C 20 - 氧杂烷基,任选取代的C 5 -C 12 - 环烷基或任选取代的C 7 -C 20 - 芳烷基,X是-NCO - , - NH-CO 2 R 1 - , - NHCO 2 R 2 - 或 - NHCOCl-基,其中R 1和R 2可以相同或不同,并且是直链 链或支链C1-C20烷基或C5-C12环烷基,以及它们的制备方法。 2-(烷氧基甲基) - 戊烷-1,5-二氨基甲酸酯或2-(烷氧基甲基) - 戊烷-1,5-二氨基酰氯适于制备2-(烷氧基甲基) - 戊烷-1,5-二异氰酸酯, 其又用于使用多异氰酸酯加成聚合方法制备塑料。

    Multiple-step process for the preparation of hexamethylene
diisocyanate-1,6 and/or isomeric aliphatic diisocyanates with six
carbon atoms in the alkylene residue
    44.
    发明授权
    Multiple-step process for the preparation of hexamethylene diisocyanate-1,6 and/or isomeric aliphatic diisocyanates with six carbon atoms in the alkylene residue 失效
    用于制备在亚烷基残基中具有6个碳原子的六亚甲基二异氰酸酯-1,6-和/或异构脂族二异氰酸酯的多步法

    公开(公告)号:US4596678A

    公开(公告)日:1986-06-24

    申请号:US600143

    申请日:1984-04-13

    CPC classification number: C07C263/04

    Abstract: Hexamethylene diisocyanate and/or isomeric alkylene diisocyanates having 6 carbon atoms in the alkylene radical, preferably 2-methylpentamethylene 1,5-diisocyanate and/or 2-ethyltetramethylene 1,4-diisocyanate are prepared without the use of phosgene in a multiple-step process by means of(a) reacting hexamethylene 1,6-diamine and/or isomeric alkylene diamines having 6 carbon atoms in the alkylene radical with urea and alcohol in the presence of dialkyl carbonate and/or carbamic acid alkyl ester as well as, in some cases, catalysts to form hexamethylene 1,6-dialkylurethane and/or isomeric alkylene dialkylurethanes having 6 carbon atoms in the alkylene radical,(b) separation and return to reaction step (a) of alcohol, dialkyl carbonate, and/or carbamic acid alkyl ester from the reaction mixture(c) evaporation of the hexamethylene 1,6-dialkylurethane and/or isomeric alkylene dialkylurethanes having 6 carbon atoms in the alkylene radical,(d) cleavage of the vaporized diurethanes into hexamethylene diisocyanate and/or isomeric alkylene diisocyanate having 6 carbon atoms in the alkylene radical and alcohol, and(e) fractional condensation of the cleavage products.

    Abstract translation: 在多步法中不使用光气制备在亚烷基中具有6个碳原子的六亚甲基二异氰酸酯和/或异构亚烷基二异氰酸酯,优选2-甲基五亚甲基-1,5-二异氰酸酯和/或2-乙基四亚甲基1,4-二异氰酸酯 通过(a)在碳酸二烷基酯和/或氨基甲酸烷基酯的存在下,使亚烷基中的六亚甲基1,6-二胺和/或具有6个碳原子的异构亚烷基二胺与脲和醇反应,以及在一些 情况下,在亚烷基中形成具有6个碳原子的六亚甲基1,6-二烷基氨基甲酸酯和/或异构亚烷基二烷基氨基甲酸酯的催化剂,(b)分离并返回到醇,碳酸二烷基酯和/或氨基甲酸烷基酯的反应步骤(a) (c)在亚烷基中蒸发具有6个碳原子的六亚甲基1,6-二烷基氨基甲酸酯和/或异构亚烷基二烷基氨基甲酸酯,(d)将汽化的二氨基甲酸酯裂解成h 亚烷基二异氰酸酯和/或亚烷基和醇中具有6个碳原子的异构亚烷基二异氰酸酯,和(e)裂解产物的分级缩合。

    Preparation of carbamates
    46.
    发明授权
    Preparation of carbamates 失效
    氨基甲酸酯的制备

    公开(公告)号:US4537960A

    公开(公告)日:1985-08-27

    申请号:US529037

    申请日:1983-09-02

    CPC classification number: C07D295/13

    Abstract: N- and O-substituted carbamates are prepared by reacting urea with an aminopropanol at 140.degree. C. or above. The compounds obtained by the novel process are useful starting materials for the preparation of textile finishing agents, stabilizers, plasticizers, dyes and crop protection agents.

    Abstract translation: N-和O-取代的氨基甲酸酯通过使脲与氨基丙醇在140℃或更高温度下反应来制备。 通过新方法获得的化合物是用于制备纺织整理剂,稳定剂,增塑剂,染料和作物保护剂的起始材料。

    Preparation of tertiary alcohols
    48.
    发明授权
    Preparation of tertiary alcohols 失效
    叔醇的制备

    公开(公告)号:US4493801A

    公开(公告)日:1985-01-15

    申请号:US317001

    申请日:1981-11-02

    CPC classification number: C07C255/00 C07C29/00 C07C29/50

    Abstract: Tertiary alcohols are prepared by oxidizing tertiary aldehydes with oxygen at elevated temperatures.The tertiary alcohols prepared in this way are valuable and versatile intermediates for dyes, drugs and crop protection agents and are used, for example, in the preparation of agrochemicals.

    Abstract translation: 在高温下用氧气氧化叔醛制备叔醇。 以这种方式制备的叔醇是用于染料,药物和作物保护剂的有价值和通用的中间体,并且用于例如农药的制备。

    Process for the preparation of an aryl mono-, di-, and/or polyurethane
    50.
    发明授权
    Process for the preparation of an aryl mono-, di-, and/or polyurethane 失效
    芳基单 - ,二 - 和/或聚氨酯的制备方法

    公开(公告)号:US4375000A

    公开(公告)日:1983-02-22

    申请号:US135242

    申请日:1980-03-31

    CPC classification number: C07C271/06

    Abstract: A process for the preparation of an aryl mono-, di-, and/or polyurethane comprising the steps of A. reacting a primary aromatic mono-, di-, and/or polyamine with an O-alkyl carbamate in the presence of an alcohol at temperatures greater than 160.degree. C., andB. separating the ammonia and other by-products from the aryl mono-, di-, and/or polyurethane.The reaction is preferably carried out in the presence of urea. The aryl mono-, di-, and/or polyurethanes produced are valuable end and intermediate products. They can be transferred into the corresponding isocyanates which can then be used for the preparation of polyurethanes.

    Abstract translation: 一种制备芳基单 - ,二 - 和/或聚氨酯的方法,包括以下步骤:在醇存在下使主芳族单 - ,二 - 和/或多胺与氨基甲酸O-烷基酯反应 在大于160℃的温度下,和B.将氨和其它副产物与芳基单 - ,二 - 和/或聚氨酯分离。 反应优选在尿素存在下进行。 所生产的芳基单,二和/或聚氨酯是有价值的终端和中间产物。 它们可以转移到相应的异氰酸酯中,然后可以用于制备聚氨酯。

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