GB880484A - Di-[benzimidazyl-(2)]-ethylene compounds - Google Patents
Di-[benzimidazyl-(2)]-ethylene compoundsInfo
- Publication number
- GB880484A GB880484A GB28149/58A GB2814958A GB880484A GB 880484 A GB880484 A GB 880484A GB 28149/58 A GB28149/58 A GB 28149/58A GB 2814958 A GB2814958 A GB 2814958A GB 880484 A GB880484 A GB 880484A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- compound
- reacting
- ethylene
- acid
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/20—Two benzimidazolyl-2 radicals linked together directly or via a hydrocarbon or substituted hydrocarbon radical
Abstract
A detergent composition contains, as an optical brightening agent, a di-[benzimidazolyl-(2)]-ethylene compound of the formula:- <FORM:0880484/III/1> in which m and n represent whole numbers of at most 2, or a sulphate, hydrochloride, acetate or tartrate of such compound. In an example an aqueous slurry of sodium lauryl sulphate, sodium dodecylbenzenesulphonate, sodium tri-polyphosphate, sodium sulphate and a compound of the above general formula is spray dried to give a detergent powder.ALSO:The invention comprises di-[benzimidazyl-(2)]-ethylene compounds having the formula <FORM:0880484/IV (b)/1> in which m and n represent whole numbers of at most 2. The compounds are prepared (1) by reacting a compound having the formula <FORM:0880484/IV (b)/2> with a glycerol-a -chlorohydrin, or with ethylene chlorohydrin, when m and n are both equal to 2; (2) by saponi-fication of a compound of the formula <FORM:0880484/IV (b)/3> (3) by dehydrating a compound of the formula <FORM:0880484/IV (b)/4> (4) by dehydrohalogenating a compound of the formula <FORM:0880484/IV (b)/5> (5) by dehydrating a compound of the formula <FORM:0880484/IV (b)/6> (6) by reacting a compound of the formula <FORM:0880484/IV (b)/7> in the molecular ratio of 2:1 with thiomalic acid or aspartic acid or functional derivatives thereof; (7) by reacting a compound of the formula <FORM:0880484/IV (b)/8> with fumaric acid or with a fumaric acid dialkyl ester; and (8) by reacting a carboxylic acid of the formula <FORM:0880484/IV (b)/9> or a functional derivative thereof, with a diamine of the formula <FORM:0880484/IV (b)/100> The products may be converted into salts with sulphuric, hydrochloric, acetic and tartaric acids.ALSO:Di - [benzimidazolyl - (2)]-ethylene compounds having the formula <FORM:0880484/IV (c)/1> in which m and n represent whole numbers of at most 2, are used to brighten cotton, regenerated cellulose, cellulose di- or triacetate, polyamide, polyacrylonitrile and polyester fibres. The compounds are prepared (1) by reacting a compound of the formula <FORM:0880484/IV (c)/2> with glycerol-a -chlorohydrin, or with ethylene chlorohydrin when m and n are both equal to 2; (2) by saponification of a compound of the formula <FORM:0880484/IV (c)/3> (3) by dehydrating a compound of the formula <FORM:0880484/IV (c)/4> (4) by dehydrohalogenating a compound of the formula <FORM:0880484/IV (c)/5> (5) by dehydrating a compound of the formula <FORM:0880484/IV (c)/6> (6) by reacting a compound of the formula <FORM:0880484/IV (c)/7> in the moleculor ratio of 2 : 1 with thiomalic acid or aspartic acid or functional derivatives thereof; (7) by reacting a compound of the formula <FORM:0880484/IV (c)/8> with fumaric acid or with a fumaric acid dialkylester and (8) by reacting a carboxylic acid of the formula <FORM:0880484/IV (c)/9> or a functional derivative thereof, with a diamine of the formula <FORM:0880484/IV (c)/100>
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH880484X | 1957-09-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB880484A true GB880484A (en) | 1961-10-25 |
Family
ID=4544800
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB28149/58A Expired GB880484A (en) | 1957-09-02 | 1958-09-02 | Di-[benzimidazyl-(2)]-ethylene compounds |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE570835A (en) |
FR (1) | FR1209554A (en) |
GB (1) | GB880484A (en) |
-
0
- BE BE570835D patent/BE570835A/xx unknown
-
1958
- 1958-08-14 FR FR1209554D patent/FR1209554A/en not_active Expired
- 1958-09-02 GB GB28149/58A patent/GB880484A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR1209554A (en) | 1960-03-02 |
BE570835A (en) |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB750155A (en) | Substituted alanines | |
GB1059256A (en) | Fluorescent, practically colourless, benzimidazole and benzoxazole derivatives | |
GB1101156A (en) | Triazole derivatives and their use as optical whitening agents | |
GB880484A (en) | Di-[benzimidazyl-(2)]-ethylene compounds | |
US2385571A (en) | Making n-sulphonylureas | |
GB1113918A (en) | 7-v-triazolyl-(2)-coumarin compounds | |
GB1087375A (en) | Carbostyril brightening agents | |
US2073052A (en) | Manufacture of cellulose derivatives and in plastic products, etc. | |
GB924762A (en) | New derivatives of 1,4-bis-styryl-benzene and optical brightening therewith | |
ES449817A1 (en) | Substituted 2-phenylimino-thiazolines a process for their preparation and their use as ectoparasiticides | |
GB671141A (en) | Terephthalamide derivatives | |
GB911344A (en) | Iodinated 4-(4-alkoxyphenoxy) phenylpropionic acids and pharmaceutically acceptable salts thereof | |
GB811816A (en) | Heterocyclic hydrazides | |
SU617465A1 (en) | Complexes of bivalent iron with derivatives of 5-nitroso-6-oxyquinoline as dyes for natural and synthetic polyamide fibres | |
GB668235A (en) | Process for the preparation of methionine derivatives | |
GB855022A (en) | Improvements in and relating to carbostyril derivatives | |
GB1107036A (en) | Esters of dibenzocycloheptenyl-carboxylic acids | |
GB940140A (en) | Improvements in or relating to a process for the preparation of ยช -cyclopropane acrylic acids or derivatives thereof | |
ES269515A1 (en) | Ethers of methyl 18-epi-reserpate and salts thereof and process for their manufacture | |
GB563991A (en) | Improvements in or relating to the production of polyvinyl compounds | |
GB834903A (en) | Method of optically brightening materials | |
GB886437A (en) | Improvements in or relating to basic esters of etherified benzilic acids | |
GB669348A (en) | Purification of streptomycin | |
JPS54125687A (en) | Pirazine derivative and its preparation | |
GB764185A (en) | Therapeutically active double salts of dicarboxylic acids and salicylic acid derivatives |