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    • 72. 发明授权
    • Organic reagents and process of preparing same
    • 有机试剂及其制备方法
    • US4085261A
    • 1978-04-18
    • US545220
    • 1975-01-29
    • Avraham PatchornikAbraham WarshawskyMatityahu FridkinRami Kalir
    • Avraham PatchornikAbraham WarshawskyMatityahu FridkinRami Kalir
    • B01J45/00C07C45/68C07C205/22C07D213/06C07D213/16C07D215/24C07D215/26C08F8/00C08F8/24C08F8/30C08F212/00C22B3/26B01D11/00C08C19/00C08F232/00
    • C07D213/16B01J45/00C07C205/22C07C205/45C07C45/68C07D213/06C07D215/24C07D215/26C08F8/24C08F8/30C22B3/0097C22B3/42Y02P10/234
    • A process for producing reagents useful in organic synthesis, for removing metal values from solutions thereof, for the capture of aldehydes, of the general formula ##STR1## wherein Z designates a recurring part (CH.sub.2 --CH--CH.sub.2 -- of a polymeric backbone of a polymer like polystyrene, of a copolymer comprising polystyrene and divinylbenzene, and butadiene, or other copolymers comprising styrene moieties; or wherein Z is the aliphatic moiety of a long-chain aralkyl compound having a terminal aryl group; or wherein Z designates alkyl; corresponding compounds wherein instead of the optionally substituted phenyl group there is present an optionally substituted naphthyl group; wherein n is an integer of from 1 to 15, and wherein Q designates a group selected from: ##STR2## wherein R designates --H, lower alkyl, aryl, which may be substituted and wherein R" designates --H, alkyl, aryl, halogen, nitro or carboxy, or ##STR3## wherein R is --H, lower alkyl, aryl (which may be substituted), R.sub.1 is --H, alkyl, aryl (which may be substituted), R.sub.2 is --H, alkyl, aryl or substituted aryl, and wherein Y is --H or a non-interfering substituent;which comprises chemically binding an activated chemical moiety to a group Z- -, or a corresponding naphthyl-containing group, wherein Z is as defined above, according to the reaction scheme: ##STR4## wherein Q is as defined above, or a functional group which can be converted to such group after the chemical bonding; and X is --Cl or --Br.
    • 用于生产有机合成中的试剂的方法,用于从其溶液中除去金属,用于捕获醛,通式为“IMAGE”,其中Z表示重复部分(CH2-CH-CH2- 聚苯乙烯,包含聚苯乙烯和二乙烯基苯的共聚物,丁二烯或包含苯乙烯部分的其它共聚物;或其中Z是具有末端芳基的长链芳烷基化合物的脂族部分;或其中Z表示烷基;相应的化合物 其中代替任选取代的苯基,存在任选取代的萘基;其中n为1至15的整数,并且其中Q表示选自以下的基团: 其中R表示-H,可以被取代的低级烷基,芳基,其中R“表示-H,烷基,芳基,卤素,硝基或羧基,或者” IMAGE> wherei n为低级烷基,芳基(其可被取代),R 1为-H,烷基,芳基(其可被取代),R 2为-H,烷基,芳基或取代的芳基,并且其中Y为-H 或非干扰性取代基; 其包括根据反应方案将活化的化学部分与基团Z-或相应的含萘基团(其中Z如上所定义)化学结合:其中Q如上所定义 或在化学键合后可以转化为这种基团的官能团; X是-Cl或-Br。
    • 75. 发明授权
    • Photographic developing agents
    • 照相显影剂
    • US3970454A
    • 1976-07-20
    • US537221
    • 1974-12-30
    • Claude Fernand Marcel Gerbal
    • Claude Fernand Marcel Gerbal
    • C07D215/26C07D215/38G03C5/30C07D215/00C07D215/12C07D215/58
    • G03C5/3021C07D215/26C07D215/38
    • A new class of photographic developing agents of the p-aminophenol type are compounds of the formula: ##EQU1## wherein R.sup.1 is an alkyl group of 1 to 12 carbon atoms;R.sup.2 is an alkyl group of 1 to 12 carbon atoms or a sulfoalkyl group of 1 to 12 carbon atoms,R.sup.3 is a hydrogen atom or an alkyl group of 1 to 12 carbon atoms,R.sup.4 is a hydrogen atom or an alkyl group of 1 to 12 carbon atoms, and X.sup.- is an anion with the proviso that when R.sup.2 is a sulfoalkyl group then X.sup.- is the sulfo radical of R.sup.2.These compounds are useful as color developing agents, especially in diffusion transfer processes, and have been found to provide advantageous characteristics as compared with conventional developers of the p-amino-phenol type, for example, a substantial decrease in the formation of unwanted color stain in the receiving layer employed in diffusion transfer processes.
    • 一类新型对氨基苯酚型照相显影剂是下式的化合物:R1R2 ANGLE N ANGLE CH2 CH2 CH2 CH2 CH2 CH2其中R1是1-12个碳原子的烷基; R2为碳原子数为1〜12的烷基或碳原子数1〜12的磺基烷基,R3为氢原子或碳原子数为1〜12的烷基,R4为氢原子或1〜 12个碳原子,而X - 为阴离子,条件是当R 2为磺基烷基时,则X 1为R 2的磺基。
    • 79. 发明授权
    • Organic ammonium salts of vinyl sulfonic acid
    • 乙烯基磺酸的有机铵盐
    • US3236881A
    • 1966-02-22
    • US8097861
    • 1961-01-06
    • BASF AG
    • HARRY DISTLERWERNER MUELLERULRICH WERNER HEINZ
    • C07C41/16C07C209/18C07C309/20C07D213/20C07D215/10C07D215/26C07D295/02C07D295/037C07D295/04C07D521/00C08F28/00
    • C07D295/037C07C209/18C07C309/20C07C319/18C07C2601/14C07D213/20C07D215/10C07D215/26C07D231/12C07D233/56C07D249/08C07D295/02C07D295/04C08F28/00Y10S526/923C07C323/66
    • Aqueous polymer dispersions are prepared from salts of vinyl sulphonic acid with organic nitrogen bases. The salts have the formula where R1 is a monovalent hydrocarbon radical which may be substituted by halogen or a hydroxyl group or acylated hydroxyl group or may contain ether linkages; R2, R3, and R4 may be as R1 or may be hydrogen; R4 may be a hydrocarbon radical substituted by a group of formula R1 and R2 may be polymethylene groups which connect the nitrogen atom of formula I with a group of formula the substituents R5, R6 and R7 being hydrogen, hydrocarbon radicals or hydroxyalkyl radicals, and A(-) an anion, particularly that of vinyl sulphonic acid; R2 and R3 may form a 5 to 7 membered heterocyclic ring with the nitrogen atom of formula I; and R1, R2 and R3 may be components of a 5 or 6 membered ring containing the nitrogen atom of formula I. In Examples A to E aqueous dispersions of copolymers are prepared from:-trimethyl-phenyl-ammonium vinyl sulphonate and n-butyl acrylate; trimethyl-cyclohexyl-ammonium vinyl sulphonate, vinyl acetate and n-butyl acrylate; methyl-triethanol-ammonium-vinyl sulphonate, vinyl propionate and n-butyl acrylate; a salt derived from vinyl sulphonic acid methyl ester and the reaction product of 1 mol. of diethylamine with 4 mols. of ethylene oxide, ethyl acrylate and vinylidene chloride; diethyl ammonium vinyl sulphonate, ethyl acrylate and acrylic acid; potassium persulphate is used to initiate the copolymerization.ALSO:The invention comprises salts of vinyl sulphonic acid with organic nitrogen bases. The salts have the formula where R1 is a monovalent hydrocarbon radical which may be substituted by halogen or a hydroxyl group or acylated hydroxyl group or may contain ether linkages; R2, R3, and R4 may be as R1 or may be hydrogen; R4 may be a hydrocarbon radical substituted by a group of formula R1 and R2 may be polymethylene groups which connect the nitrogen atom of formula I with a group of formula R5, R6 and R7 being hydrogen, hydrocarbon radicals or hydroxyalkyl radicals, and A(-) an anion, particularly that of vinyl sulphonic acid; R2 and R3 may form a 5 to 7 membered heterocyclic ring with the nitrogen atom of formula I; and R1, R2 and R3 may be components of a 5 or 6 membered ring containing the nitrogen atom of formula I. The salts may be prepared by neutralizing the nitrogen base with vinyl sulphonic acids; or by reacting the nitrogen base with a vinyl sulphonic acid ester, the hydrocarbon radical of the alcoholic component of the ester being transferred to the nitrogen atom. In examples there are prepared salts including N-methyl-8-hydroxyquinolinium vinyl sulphonate, ethyl-dimethylanilinium vinyl sulphonate, salts from ethyl and butyl esters of vinyl sulphonic acid and 4,41-bis-(dimethylamino-diphenyl)methane, trimethylcyclohexylammoniumvinyl sulphonate, salt of dimethyl palm kernel fatty amine, N-methyl-pyridinium vinyl sulphonate, N-methyl-quinolinium vinyl sulphonate, Nmethyl-vinylimidazolium vinyl sulphonate, Nmethyl-g -picolinium p vinyl sulphonate, Nmethyl-quinaldinium vinyl sulphonate; salts of vinyl sulphonic acid and pyridine, crotylamine, 4-isopropyl-aniline, a -naphthylamine, 4-methoxy-N,N- dimethylaniline, 1-hydroxy2-amino-propane, piperazine, N-methyl pyrrole, pyrazole, thiazole, oxazole, morpholine, thiomorpholine, hexamethylene imine, diphenylamine, N- methylpyrrolidine, methyl oxazolidine, alkoxyamines, alkanolamines, reaction products of alkylene oxides with amines; and salts from simple amines and diamines.