欧盟法规
ECHA物质ECHA物质C&L通报REACH预注册上下游产品
5-chloro-4-methoxy-1,3-dinitrobenzene 1,2-dichloro-3,5-dinitrobenzene 1-chloro-2,3,5-trinitro-benzene N-ethyl-N'-(2-chloro-4,6-dinitro-phenyl)-N-nitro-ureaN-ethyl-N'-(2-chloro-4,6-dinitro-phenyl)-N-nitro-urea 1-chloro-2-iodo-3,5-dinitrobenzene acetic acid-(2-chloro-4,6-dinitro-anilide) N-(6-chloro-2,4-dinitrophenyl)benzamide 3-(2-chloro-4,6-dinitro-phenyl)-2-thioxo-thiazolidin-4-one 合成工艺路线路线简述
- 合成目标产物 2-Chloro-4,6-Dinitroaniline 主要起始原料 2,4-Dinitroaniline
- (文献来源)合成步骤主要原料 2,4-Dinitroaniline
6-氯-2,4-二硝基苯酚置于乙醇,氨,N,N-二乙基苯胺体系中,化学反应生成2-氯-4,6-二硝基苯胺
参考文献:Ullmann; Sane,Chemische Berichte,1911,Vol. 44,P. 3734
标题:Ullmann; Sane,Chemische Berichte,1911,Vol. 44,P. 3734
专利信息
专利号:US-7060818-B2
优先权日:2003-02-21
标题:Synthesis of macrocyclic tetraamido compounds and new metal insertion process
发明人:HORWITZ COLIN P; GHOSH ANINDYA
权利人:UNIV CARNEGIE MELLON
摘要:An improved method of synthesizing a macrocyclic tetraamido compound includes protecting the amino portion of an amino carboxylic acid to form a protected amino carboxylic acid; exposing the protected amino carboxylic acid to a first solvent, preferably a hydrocarbon solvent, such as toluene or 1,2-dichloroethane, dichloromethane, dibromomethane and 1,2-dibromoethane. The carboxylic acid portion of the protected amino carboxylic acid is then converted to an activated carboxylic acid by one of esterification or acid halide formation, to form a protected amino activated carboxylic acid derivative. The protected amino activated carboxylic acid derivative is reacted with a diamine in the presence of a second solvent, such as THF or ,2-dichloroethane, dichloromethane, dibromomethane and 1,2-dibromoethane, to form a protected diamide diamine intermediate. Following deprotection, the diamide diamine intermediate is reacted with an activated diacid, such as an activated malonate, oxalate or succinate derivative to form the macrocyclic tetraamido compound. The macrocyclic tetraamido compound may further be complexed with a transition metal.
专利号:US-4118384-A
优先权日:1976-02-21
标题 :Process for preparation of azo dyestuffs by coupling in presence of aromatic sulphonic acid-formaldehyde reaction product
发明人:MOLLS HANS-HEINZ; SCHIWY WILLY; HORNLE REINHOLD; NEBELING REINHARD
权利人:BAYER AG
摘要:Dyestuff dispersions and dyestuff solutions free from salt or at least having a low salt content are obtained in that the diazotization is carried out with addition of free dispersing agent acid to which, after the synthesis, either no basic agents are added or basic agents are added only up to a pH value of 3. The disclosed process gives dyestuff compositions of low salt content and results in readily dispersible dyestuffs when water insoluble dyestuffs are prepared and stable solutions when water soluble dyestuffs are prepared. The process is widely applicable and chemical constitution of the dyestuffs is conventional.
专利号:US-4035350-A
优先权日:1975-01-30
标 题:Process for the preparation of water-soluble azo dyestuffs by reacting an aromatic amine and a coupling component with alkali metal nitrite or alkyl nitrite in the absence of acid
发明人:LANDLER JOSEF; WORFEL ERHARD
权利人:HOECHST AG
摘要:A new and very advantageous Process had been found for the preparation of azo dyestuffs by diazotation and coupling in which the synthesis is carried out without the hitherto usual addition of an acid, with the proviso that at least one of the diazo and coupling components contains at least one acid group. Besides the saving of reaction material and subsequently of alkali for neutralization of the reaction medium and isolation of the dyestuff, highly concentrated solutions of the dyestuff and salt-free or practically salt-free dyestuffs can be obtained, and waste-water is no longer charged with big amounts of salts.
专利号:CN-105461572-B
优先权日:2014-12-29
标 题:A kind of cleaning process for continuous synthesis of 2,4-dinitro-6-chloroaniline
专利号:US-2004167329-A1
优先权日:2003-02-21
标 题:Synthesis of macrocyclic tetraamido compounds and new metal insertion process
专利号:CN-110963925-A
优先权日:2019-12-30
标 题 :Synthesis of 6-chloro-2,4-dinitroaniline by chlorine hydrogen peroxide method