Abstract:
A fluorine-containing multifunctional ester compound represented by the formula ##STR1## wherein A is halogen atom, NO.sub.2 or N.sub.3, B is halogen atom or SR.sup.2, R.sup.1 is lower aliphatic group, aromatic group or aralkyl, R.sup.2 is lower aliphatic group or aromatic group.
Abstract:
An optically active or racemic 2-amino-5-hydroxy-1,2,3,4-tetrahydronaphthalene wherein the nitrogen atom of the amino group carrier two alkyl groups, one of which is unsubstituted and the other is substituted by at least one functional group, or a physiologically hydrolysable ester thereof in free base form or in the form of an acid addition salt thereof is provided which is active against heart circulatory disorders and Morbus Parkinson and inhibits prolactin secretion inhibition.
Abstract:
A process for preparing a 2,6-bis-[(4-azidophenyl)methylene]-cyclohexanone of the formula ##STR1## wherein R is hydrogen or alkyl of 1-6 C atoms, comprises condensing a cyclohexanone of the formula ##STR2## wherein R is as defined above, with 4-aminobenzaldehyde, the 4-amino group optionally being protected, in the presence of an alkaline condensing agent; removing the protective group when the 4-amino group is protected; diazotizing the resultant 2,6-bis-[(4-aminophenyl)methylene]-cyclohexanone of the formula ##STR3## wherein R is as defined above, and reacting the diazotization product with an alkali metal azide.
Abstract:
Production of carbonyl compounds substituted in the .alpha.-position and having the formula: ##EQU1## wherein R.sup.1 is alkyl, aralkyl, phenyl, toluyl, naphthyl, alkoxy or amino; R.sup.2 is hydrogen ##EQU2## A is hydrogen, alkyl, halo or ##EQU3## R.sup.6 is hydrogen or methyl, and R.sup.11 is alkyl; wherein said compounds are formed by reacting a sulfur ylide having the formula: ##EQU4## wherein Y is the radical ##EQU5## and R.sup.9 and R.sup.10 are alkyl or phenyl, with a solution containing both an electrophilic agent A' that is converted into the radical A and a nucleophilic agent B' that is converted into the radical B. The resulting carbonyl compounds are useful as starting materials for the production of paper, textile, and leather auxiliaries, plant protection agents, alkyd resins, polyesters and polyamides.
Abstract translation:制备在α-位取代的具有下式的羰基化合物:其中R1是烷基,芳烷基,苯基,甲苯基,萘基,烷氧基或氨基; R2是氢R6R6O R6R6O || PARALLEL || PARALLEL -CH-CH-CN,-C-R1或-CH-CH-C-OR11; A是氢,烷基,卤素或R6R6 | -CH-CH-CN R6是氢或甲基,R11是烷基; 其中所述化合物通过使具有下列结构式的硫叶立德反应形成:其中Y是基团CH 3 R 9 = S ANGLE或= S ANGLE PARALLEL OCH 3 R 10,R 9和R 10是烷基或苯基,与 含有转化为自由基A的亲电子试剂A'和转化为自由基B的亲核试剂B'的溶液。得到的羰基化合物可用作生产纸,纺织品和皮革助剂的原料 植物保护剂,醇酸树脂,聚酯和聚酰胺。
Abstract:
NEW AND VALUABLE SUBSTITUTED DINITROANILINES HAVING A GOOD HERBICIDAL ACTION AND A PROCESS FOR CONTROLLING THE GROWTH OF UNWANTED PLANTS WITH THESE COMPOUNDS.
Abstract:
DISCLOSED ARE NITROGEN CONTAINING SILANE COMPOUNDS OF THE FORMULA
(X)A-SI(-(T)B)-(R-(O-C(=O)-N3)C)D
WHERE R IS AN ORGANIC RADICAL, X IS SELECTED FROM HALO, HYDROXY, ALKOXY, ARYLOXY, ORGANO OXYCARBONYL, AZIDO, AMINE, AND AMIDE RADICALS; T IS SELECTED FROM ALKYL, CYCLOALKYL, ARYL, ALKARYL, AND ARALKYL RADICALS; A IS AN INTEGER FROM 1 TO 3; B IS AN INTEGER FROM 0 TO 2; C IS AN INTEGER FROM 1 TO 10; D IS AN INTEGER FROM 1 TO 3; AND A+B+D EQUALS 4;
-OOC-C(-R'')-N2, -OOC-N3, AND -SO2-N3
WHERE R'' IS SELECTED FROM HYDROGEN, ALKYL, CYCLOALKYL, ARYL AND -COOR" RADICALS; WHERE R" IS SELECTED FROM ALKYL, CYCLOALKYL, AND ARYL RADICALS.
Abstract:
DIMERIC AZIDOPHOSPHA (III)-CARBORANES ARE PREPARED BY REACTING A DIMERIC HALOPHOSPHA (III)-CARBORANE, SUCH AS:
CL-P WITH AN ALKALI METAL AZIDE SUCH AS SODIUM AZIDE IN THE PRESENCE OF AN INORGANIC LIQUID AND A TEMPERATURE RANGING FROM ABOUT -20*C. TO ABOUT +80*C. THE DIMERIC AZIDOPHOSPHA (III)-CARBORANES CAN BE CONDENSED WITH A DIPHOSPHINE TO YIELD VALUABLE POLYMERIC MATERIALS WHICH, WHEN COMPOUNDED WITH INERT MINERAL FILLERS AND PRESSURE MOLDED, ARE SUITABLE FOR USE IN HIGH PRESSURE AND HIGH TEMPERATURE APPLICATIONS.
Abstract:
There is provided the compound 4-azido-4,4-dinitro-1-butanol (ADNBOH) and a method for making same which comprises reacting trinitromethane and acrolein at a reduced temperature to provide 4,4,4-trinitro-butyraldehyde (TNBAl), reducing the TNBSl to provide 4,4-trinitro-1-butanol (TNBOH) which is further reduced to provide 4,4-dinitro-1-butanol (DNBOH), reacting the DNBOH with acetyl chloride to provide 4,4-dinitro-1-butyl acetate (DNBAc), reacting the DNBAc with an alkali metal azide in an electrolysis cell to provide 4-azido-4,4-dinitro-1-butyl acetate (ADNBAc) and reacting the ADNBAc with a lower alcohol and recovering the 4-azido-4,4-dinitro-1-butanol (ADNBOH).Also provided are several azidodinitro derivatives of 4-azido-4,4-dinitro-1-butanol and methods for making same.