GB479898A - Manufacture of isocyclic compounds - Google Patents
Manufacture of isocyclic compoundsInfo
- Publication number
- GB479898A GB479898A GB148438A GB148438A GB479898A GB 479898 A GB479898 A GB 479898A GB 148438 A GB148438 A GB 148438A GB 148438 A GB148438 A GB 148438A GB 479898 A GB479898 A GB 479898A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- products
- treating
- residue
- oxygen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Landscapes
- Detergent Compositions (AREA)
Abstract
Products stated to have wetting, foaming, dispersing, and cleansing properties are obtained by treating with a halide or anhydride of sulphuric acid or with amidosulphonic acid, a compound having the formula R.X.Y wherein R is an aromatic or hydroaromatic residue containing as a substituent at least one hydrocarbon residue with at least 3 carbon atoms, X is an alkyl residue united directly or by means of oxygen, nitrogen or sulphur with R, in the chain of which alkyl residue there may be one or more oxygen atoms and Y is NH2 or NHR<1> in end position in X, R<1> being an aliphatic hydrocarbon radicle. The products may be used in association with other washing agents, e.g. phosphoric acid salts or bleaching agents or with common salt or sodium sulphate. In an example, cyclohexylphenoxyethyl amine, which is prepared by treating cyclohexyl phenylglycol with thionylchloride and reacting the product with alcoholic ammonia, is converted into the sulphamic acid by means of chlorsulphonic acid in chloroform. The use of dibutylphenylethylamine, isohexyl phenylethylamine, and products obtained by reacting alkylated aromatic hydroxy or amino compounds with ethyleneimine or its homologues is mentioned. Samples have been furnished under Sect. 2(5) of products obtained by treating p-butylcyclohexylbutylamine with sulphurtrioxide, dodecylaminoethylaniline with amidosulphonic acid and a base obtained from methylamine and p-tert: octylphenyltriglycolether chloride with chlorsulphonic acid. Dodecylaminoethylaniline is obtained by condensing aniline with dodecylalcohol in the presence of zinc chloride and treating the dodecylaniline with ethyleneimine.ALSO:Products stated to have dispersing properties are obtained by treating with a halide or anhydride of sulphuric acid or with amidosulphonic acid, a compound having the formula R.X.Y, wherein R is an aromatic or hydroaromatic residue containing as a nuclear substituent at least one hydrocarbon residue with at least 3 carbon atoms, X is an alkyl residue united directly or by means of oxygen, nitrogen or sulphur with R, in the chain of which alkyl residue there may be one or more oxygen atoms and Y is NH2 or NHR<1> in end position in X, R<1> being an aliphatic hydrocarbon radicle. The products may be used in association with washing agents, e.g. phosphoric acid salts, or bleaching agents or with common salt or sodium sulphate. In an example, cyclohexylphenoxyethylamine is converted into the sulphamic acid by means of chlorsulphonic acid. The use of dibutylphenylethylamine, isohexyl phenylethylamine and products obtained by reacting alkylatedaromatic hydroxy or amino compounds with ethylenediamine or its homologues is mentioned.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB148438A GB479898A (en) | 1936-06-05 | 1936-06-05 | Manufacture of isocyclic compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB148438A GB479898A (en) | 1936-06-05 | 1936-06-05 | Manufacture of isocyclic compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB479898A true GB479898A (en) | 1938-02-07 |
Family
ID=9722814
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB148438A Expired GB479898A (en) | 1936-06-05 | 1936-06-05 | Manufacture of isocyclic compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB479898A (en) |
-
1936
- 1936-06-05 GB GB148438A patent/GB479898A/en not_active Expired
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0127132A1 (en) | Use of alkenylsuccinic monoamides as corrosion inhibitors | |
GB833082A (en) | An improved surface-active composition | |
US2438092A (en) | Nu-sulfodicarboxylic acid aspartates | |
GB479898A (en) | Manufacture of isocyclic compounds | |
US2818388A (en) | Corrosion inhibition | |
US3341458A (en) | N-substituted amides of hydroxyethoxy-acetic acid and processes for using same | |
GB799045A (en) | Compositions containing n, n-alkylene-urea compounds | |
DE805521C (en) | Process for the preparation of quaternary ammonium compounds | |
US1931806A (en) | Process for the production of sulphuric esters of nitrogen-containing organic compounds | |
US2190733A (en) | Manufacture of alkyl substituted aryl sulphates | |
DE269938C (en) | ||
GB481557A (en) | Manufacture of isocyclic compounds | |
GB567353A (en) | Improvements in the manufacture of tetrazole compounds | |
GB443902A (en) | New textile assistants | |
GB680952A (en) | Improvements in new morphine derivatives and production thereof | |
US2414950A (en) | Conversion of biguanide salts | |
GB744505A (en) | Aqueous suspension for improving the adhesive power of a bituminous binder or any other hydrocarbon binder | |
US3895932A (en) | Method of inhibiting algae employing nitrogen derivatives of halogenated biphenyls | |
GB985970A (en) | Diaminoanthraquinones | |
DE681338C (en) | Process for the production of sulfonic acid salts | |
GB1106642A (en) | Fluorocarbon polyamines and their preparation | |
GB342601A (en) | Improvements in or relating to processes for the pickling of metals and the like processes | |
GB816913A (en) | Preparation of 2,2-methylene-bis-(4,6-dialkyl phenols) | |
US2043329A (en) | Wetting agents for mercerizing solutions | |
GB448469A (en) | Manufacture of water-soluble salts of imidoethers, imidothioethers or amidines |