摘要:
A process for the preparation of sulphonated phenols of general formula (I) where R1 is hydrogen, a C1-C20 alkyl group which is unsubstituted or substituted by halogen, cyano, hydroxyl, C1-C20 alkoxy, C2-C20 alkoxycarbonyl, acyloxy and/or phenyl which is unsubstituted or substituted by C1-C4 alkyl, C1-C4 alkoxy and/or halogen, R2 is hydrogen, C1-C20 alkyl or benzoyl of general formula (II) where R3 and R4 independently of one another are each hydrogen, halogen, C1-C12 alkyl, C1-C12 alkoxy, C1-C4 haloalkyl, C3-C8 cycloalkyl, C4-C12 cycloalkylalkyl, cyano, hydroxyl, or hydroxyethyl or are each phenoxy, C7-C10 phenylalkyl or phenyl which is unsubstituted or substituted by C1-C4 alkyl, C1-C4 alkoxy and/or halogen, and R5 is hydrogen or the group SO3X where X can be hydrogen, a monovalent metal or a group —N(R6)3, where each of the three radicals R6 can be independently of one another hydrogen, C1-C6 alkyl or C1-C6 hydroxy alkyl, which process comprises reacting a phenol of general formula (III) where R1 and R2 are as defined above, with a halosulphonic acid in a solvent which is a mixture of a C5-C10 aliphatic or cycloaliphatic hydrocarbon and a dialkyl carbonate of general formula (IV) R7—O—CO—O—R8 where R7 and R8 each represent independently a C1-C4 alkyl group.
摘要:
2,4-pentanedionemonosulfonic acid is prepared by reacting chlorosulfonic acid with 2,4-pentanedione, preferably in the presence of an anhydrous solvent. The method of this invention generally yields 2,4-pentanedionemonosulfonic acid in excess of about 75 percent. The noval pentanedionesulfonic acid 2,4-pentanedionemonosulfonic acid(acetylacetone sulfonic acid) is disclosed.
摘要:
A process for the continuous production of C.sub.7 -Cl.sub.2 -acyloxybenzenesulfonic acids, wherein phenol and a sulfonating reagent, diluted with an aliphatic C.sub.7 -Cl.sub.2 -carboxylic acid, is charged to the top of a continuous-flow reactor heated to 80.degree.-100.degree. and the mixture of phenolsulfonic acid and the aliphatic carboxylic acid, leaving the bottom end of this continuous-flow reactor, and a chlorinating reagent are charged to the top of a second continuous-flow reactor, nitrogen being passed in counter-current through both continuous-flow reactors.
摘要:
Processes of reducing the inorganic sulfur-containing acid and the low equivalent weight organic sulfonic acid content of an acid mass comprising organic sulfonic components and inorganic sulfonating agent contaminants are described. In general, the process comprises the steps of(a) treating the acid mass with ammonia in the presence of water to neutralize the acids in said acid mass and to form a mixture containing the ammonium salts of said acids.(b) allowing separation of the mixture to provide a lower aqueous phase containing water-soluble ammonium salts and an upper phase comprising the oleophilic alcohol and ammonium salts of the organic sulfonic acids, and(c) recovering at least a portion of said upper phase.The efficiency of the reduction of undesirable materials from the acid mass can be increased by subjecting the recovered upper phase to additional water extractions in the presence of the oleophilic alcohol.The ammonium salts of the organic sulfonic acids recovered by the above process can be converted to oil-soluble metal salts by reacting said ammonium salts with a basically reacting metal compound in such amounts and under such conditions as to form metal salts of said organic sulfonic acids. The metals salts prepared in this manner may be neutral metal salts or highly basic metal salts. The neutral and metal basic salts are useful in a variety of applications including lubricants and fuels.
摘要:
The invention relates to trisubstituted sulfohalides, the process for their preparation and their use as intermediate products for the manufacture of novel compounds.The trisubstituted sulfohalides according to the invention correspond to the following general formula (I): ##STR1## in which: X is a halogen atom, particularly bromine or preferably chlorine;R.sub.3 and R.sub.4 each represent, independently of one another, a lower alkyl radical having from 1 to 4 carbon atoms, A represents hydrogen, halogen, alkoxy radicals having from 1 to 4 carbon atoms, alkylsulfonyl groups having from 1 to 4 carbon atoms, or the group NO.sub.2, or CF.sub.3.The invention is useful in the manufacture of medicaments.
摘要翻译:本发明涉及三取代磺酰卤,其制备方法及其作为制备新化合物的中间产物的用途。 根据本发明的三取代磺酰卤对应于以下通式(I):其中:X是卤素原子,特别是溴或优选氯; R 3和R 4各自独立地表示具有1至4个碳原子的低级烷基,A表示氢,卤素,具有1至4个碳原子的烷氧基,具有1至4个碳原子的烷基磺酰基,或 组NO2或CF3。 本发明在制备药物中是有用的。
摘要:
The invention relates to an improved process for the production of 2-amino-1-naphthalenesulfonic acid (Tobias acid). This improved process makes it possible to obtain Tobias acid which has only a very low content of 2-aminonaphthalene and in high space-time yield. The process starts from 2-hydroxynaphthalene and comprises the following main reaction steps:(a) the sulfonation of 2-hydroxynaphthalene to 2-hydroxynaphthalene-1-sulfonic acid (oxy-Tobias acid) with chlorosulfonic acid, in an inert organic solvent;(b) the neutralization of the liberated hydrochloric acid and excess chlorosulfonic acid still present in the reaction medium and conversion of the 2-hydroxynaphthalene-1-sulfonic acid obtained into the corresponding ammonium salt with ammonia;(c) conversion of the 2-hydroxy group into the 2-amino group by the Bucherer reaction; and(d) the subsequent precipitation of the Tobias acid with dilute sulfuric acid.
摘要:
Phenols of the formula I ##STR1## wherein n has a value from 1 to 15,each of R.sub.1, R.sub.2, R.sub.3 and R.sub.4 independently is a hydrogen atom, a C.sub.1 - .sub.18 -alkyl group, an aryl group, a C.sub.5 -C.sub.12 -cycloalkyl group or a C.sub.7 -C.sub.13 -aralkyl group,R.sub.5 is a hydrogen atom or a C.sub.1 -C.sub.18 -alkyl group,Y is a carbonyl, thiocarbonyl, sulphinyl, sulphonyl, -P(OR.sub.7)-, -P(.dbd.O) (OR.sub.7)-, -P(.dbd.O) (R.sub.7)- or -P(R.sub.7)- group, andR.sub.6 is a radical --CHR.sub.8 --CHR.sub.9 --S--CR.sub.10 R.sub.11 R.sub.12, wherein each of R.sub.8 and R.sub.9 independently is a hydrogen atom or a C.sub.1 -C.sub.6 -alkyl group, R.sub.10 is a hydrogen atom, a C.sub.1 -C.sub.19 -alkyl group, a C.sub.2 -C.sub.4 -alkenyl group or an aryl group, R.sub.11 is a hydrogen atom or a methyl group and R.sub.12 is a hydrogen atom or a methyl group, or, if R.sub.11 is a hydrogen atom, is a C.sub.2 -C.sub.6 -alkyl group, or, if R.sub.10 is a hydrogen atom, R.sub.11 and R.sub.12 together with the carbon atom to which they are attached represent a cycloalkyl group, or R.sub.10, R.sub.11 and R.sub.12 together with the carbon atom to which they are attached represent an aryl group, or if Y is a thiocarbonyl, sulphinyl or sulphonyl group,R.sub.6 can also be a hydrogen atom or a C.sub.1 -C.sub.18 -alkyl group or an aryl group, andR.sub.7 is a hydrogen atom, a C.sub.1 -C.sub.18 -alkyl group or an aryl group,as stabilizers for organic material.
摘要:
Aromatic polyisocyanates containing sulphonic acid or sulphonate groups which are substantially free from crystalline product and a method for making them are provided wherein a mixture of aromatic polyisocyanates having an isocyanato content of from about 10% to about 42% by weight is sulphonated, the improvement which comprises mixing and reacting liquid aromatic polyisocyanates having a viscosity of from about 8 cP to about 49 cP at 25.degree. C. and containing at least 40% by weight of phosgenation products of an aniline-phosgenation condensate and at least about 20% by weight of 2,6-tolylene diisocyanate, 2,4'-diphenylmethane diisocyanate, 2,2'-diphenylmethane diisocyanate or a mixture thereof, based on the weight of said liquid aromatic polyisocyanates with a sulphonating agent in an amount equivalent to from about 0.1% to about 40% by weight sulphur trioxide, based on the weight of said liquid aromatic polyisocyanates.
摘要:
Novel substituted benzenedisulfonamides are disclosed which compounds are active anthelmintic agents being particularly useful against fascioliasis in sheep and cattle. Specifically the active compounds are 4-amino-1,3-benzenedisulfonamide with an unsaturated substituted alkyl group. Compositions and methods containing the novel substituted benzenedisulfonamides for use in anthelmintic therapy particularly against liver fluke are also disclosed.