Preparation of polycyclic aromatic compounds
    22.
    发明授权
    Preparation of polycyclic aromatic compounds 失效
    多环芳烃化合物的制备

    公开(公告)号:US3761530A

    公开(公告)日:1973-09-25

    申请号:US3761530D

    申请日:1972-05-31

    Inventor: VAN VENROOY J

    Abstract: A method for the preparation of 1,3-dimethyl substituted polycyclic aromatic compounds which comprises (1) subjecting a compound of structure

    D R A W I N G

    Abstract translation: 一种制备1,3-二甲基取代的多环芳族化合物的方法,其包括(1)使Ar为芳族或取代的芳族基团的结构化合物与丙醛进行混合醛醇缩合以形成4-Ar-2 - 甲基-2-戊烯醛,和(2)使所述戊烯醛进行由卤素酸催化的闭环。

    Dehydrocyclization of hydrocarbons
    23.
    发明授权
    Dehydrocyclization of hydrocarbons 失效
    烃的脱氢化

    公开(公告)号:US3755486A

    公开(公告)日:1973-08-28

    申请号:US3755486D

    申请日:1971-08-26

    Inventor: OISHI M BUTTE W

    CPC classification number: C07C5/373 B01J29/12 C10G35/095

    Abstract: PROCESS OF DEHYDROCYCLIZING C6-C10 HYDROCARBONS HAVING AT LEAST A C6 BACKBONE USING A LI,NA OR K ZEOLITE X OR Y OR FAUJASITE IMPREGNATED WITH 0.3 TO 1.4 PERCENT PT AT FROM 500 TO 560*C. AND PREFERABLY 510 TO 550*C. USING A PARTIAL PRESSURE OF H2 OF FROM 10 TO 300 P.S.I. AND PREFERABLY 50 TO 200 P.S.I. TO FORM BENZENE AND ALKYLBENZENES. OPTIONALLY THE CATALYST CAN BE TREATED WITH CHLORINE SO THAT IT CONTAINS FROM 0.3 TO 1.5 WEIGHT PERCENT CHLORINE WHICH IMPROVES THE EFFECTIVESS OF THE CATALYST.

    Ethylene alkylation resulting in alkylate with high proportion of 2,3-dimethylbutane
    24.
    发明授权
    Ethylene alkylation resulting in alkylate with high proportion of 2,3-dimethylbutane 失效
    亚苄基化合物的乙烯烷基化与2,3-二甲基丁二烯的高比例

    公开(公告)号:US3754052A

    公开(公告)日:1973-08-21

    申请号:US3754052D

    申请日:1972-01-14

    CPC classification number: C10L1/06

    Abstract: AN IMPROVED METHOD FOR THE PREPARATION OF 2,3-DIMETHYLBUTANE ADMIXED WITH A BRANCHED C8 ALKYLATE MIXTURE BY SULFRIC ACID ALKYLATION IS PROVIDED IN A TWO-STAGE PROCESS WHEREIN ISOBUTYLENE ARE CO-DEMERIZED IN THE PRESENCE OF ISOBUTANE AND SULFRIC ACID UNDER REACTION CONDITIONS WHICH FAVOR THE FORMATION OF 3,3-DIMETHYL-1-BUTYL SULFATE, AND THEREAFTER THE SAID 3,3-DIMETHYL-1-BUTYL SULFATE IS REACTED WITH THE ISOBUTANE UNDER CONDITION WHICH FAVOR THE FORMATION OF 2,3-DIMETHYLBUTANE. THIS PROCESS IS ADVANTAGEOUS IN THAT IT PERMITS THE INCORPORATION OF ETHYLENE INTO A SULFRIC ACID ALKYLATION REACTION WITHOUT THE FORMATION OF LARGE AMOUNTS OF UNWANTED ETHYL SULFATE.

    Polysulfonate polymers from adamantane bisphenols
    26.
    发明授权
    Polysulfonate polymers from adamantane bisphenols 失效
    来自ADAMANTANE BISPHENOLS的聚碳酸酯聚合物

    公开(公告)号:US3738965A

    公开(公告)日:1973-06-12

    申请号:US3738965D

    申请日:1971-12-30

    Inventor: THOMPSON R DULING I

    CPC classification number: C08L81/08 C08G75/24

    Abstract: WHERE R1 AND R2 ARE HYDROGEN OR HYDROCARBYL RADICAL HAVING 1 TO 20 CARBON ATOMS, AR REPRESENTS A DIVALENT AROMATIC HYDROCARBON RADICAL AND N REPRESENTS THE NUMBER OF SUCH REPEATING UNITS WHICH ARE PRODUCED. THESE THERMOPLASTIC RESINS ARE VALUABLE IN THE MANUFACTURE OF MOLDED AND EXTRUDED ARTICLES.

    PHENYLENE)-O-SO2-AR-SO2)N-
    -(O-(1,4-PHENYLENE)-(1-R1,5-R2-ADAMANTAN-7,3-YLENE)-(1,4-
    NOVEL SOLID POLYSULFONATES HAVING THE STRUCTURE:

    Ethylation of adamantane nucleus with bf{11 {0 etherate
    28.
    发明授权
    Ethylation of adamantane nucleus with bf{11 {0 etherate 失效
    ADAMANTANE NUCLEUS WITH BF {11 {0 ETHERATE

    公开(公告)号:US3671600A

    公开(公告)日:1972-06-20

    申请号:US3671600D

    申请日:1971-10-27

    Inventor: MOORE ROBERT E

    CPC classification number: C07C2/86 C07C2527/054 C07C2603/74 C07C13/615

    Abstract: Adamantane hydrocarbons of the C10-C30 range having one to four open bridgehead positions are ethylated by the reaction of a mixture of boron fluoride etherate and sulfuric acid (90-100 percent H2SO4 equivalent by weight) or fluorosulfonic acid (HFSO3) at a temperature in the range of -10* to 100* C. During the reaction, the adamantane nucleus remains intact and any alkyl groups attached thereto in the adamantane hydrocarbon charge remain at the original position. Ethylation occurs only at bridgehead positions of the nucleus and from one to four alkyl or cycloalkyl groups can be substituted if such bridgehead positions are open in the starting hydrocarbon. The ethylation product has one or more ethyl substituents than the starting hydrocarbon, which substituents are attached to the adamantane nucleus at bridgehead positions.

    Abstract translation: 具有一至四个开放桥头位置的C10-C30范围的金刚烷烃通过氟化硼醚合物和硫酸(90-100%H 2 SO 4当量重量)或氟磺酸(HFSO 3)的混合物在温度为 在-10℃至100℃的范围内。在反应过程中,金刚烷核保持完整,金刚烷烃电荷中附着的任何烷基保留在原始位置。 乙酰化仅在核的桥头位置发生,并且如果起始烃中的这种桥头位置是开放的,则1-4个烷基或环烷基可被取代。 乙基化产物与起始烃具有一个或多个乙基取代基,该取代基在桥头位置连接到金刚烷核上。

    Preparation of 2-pyrrolidone
    30.
    发明授权
    Preparation of 2-pyrrolidone 失效
    2-吡咯烷酮的制备

    公开(公告)号:US3884936A

    公开(公告)日:1975-05-20

    申请号:US35327773

    申请日:1973-04-23

    CPC classification number: C07D201/08

    Abstract: A process for preparing 2-pyrrolidone which comprises reacting maleic acid or maleic anhydride with hydrogen and ammonia in an aqueous system at a mole ratio of ammonia to acid or anhydride of from 1.0:1 to 1.2:1, at a temperature of from about 200* to about 300*C, at a pressure of from about 1,000 to about 3,000 psig, for a time of about 0.5 to about 8 hours, and in the presence of a catalyst of palladium supported on carbon.

    Abstract translation: 一种制备2-吡咯烷酮的方法,其包括使马来酸或马来酸酐与水和氨在氨水与酸或酸酐的摩尔比为1.0:1至1.2:1的水系中以约200的温度反应 在约1000至约3,000psig的压力下进行约0.5至约8小时的时间,并在负载在碳上的钯催化剂存在下进行。

Patent Agency Ranking