ES356174A1 - Procedure for obtaining a quaternary ammonium complex. (Machine-translation by Google Translate, not legally binding) - Google Patents
Procedure for obtaining a quaternary ammonium complex. (Machine-translation by Google Translate, not legally binding)Info
- Publication number
- ES356174A1 ES356174A1 ES356174A ES356174A ES356174A1 ES 356174 A1 ES356174 A1 ES 356174A1 ES 356174 A ES356174 A ES 356174A ES 356174 A ES356174 A ES 356174A ES 356174 A1 ES356174 A1 ES 356174A1
- Authority
- ES
- Spain
- Prior art keywords
- phenyl
- group
- alkyl
- benzyl
- lower alkyl
- 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
- 238000000034 method Methods 0.000 title abstract 2
- 125000001453 quaternary ammonium group Chemical group 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 9
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 4
- -1 dodecylbenzyl Chemical group 0.000 abstract 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 3
- 125000005037 alkyl phenyl group Chemical group 0.000 abstract 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 3
- 229910052794 bromium Inorganic materials 0.000 abstract 3
- 125000004799 bromophenyl group Chemical group 0.000 abstract 3
- 229910052801 chlorine Inorganic materials 0.000 abstract 3
- 239000000460 chlorine Substances 0.000 abstract 3
- 125000004803 chlorobenzyl group Chemical group 0.000 abstract 3
- 125000000068 chlorophenyl group Chemical group 0.000 abstract 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical group C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract 2
- 125000006307 alkoxy benzyl group Chemical group 0.000 abstract 2
- 125000006177 alkyl benzyl group Chemical group 0.000 abstract 2
- 125000006278 bromobenzyl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- OFXMSTYWWGEZKX-UHFFFAOYSA-N 4-methyl-3-morpholin-4-ylmorpholine Chemical group CN1CCOCC1N1CCOCC1 OFXMSTYWWGEZKX-UHFFFAOYSA-N 0.000 abstract 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000005036 alkoxyphenyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 125000006285 dibromobenzyl group Chemical group 0.000 abstract 1
- 125000006286 dichlorobenzyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 abstract 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Procedure for obtaining a quaternary ammonium complex, which responds to the general formula: **(See formula)** wherein R is selected from the group consisting of alkyl of 8 to 24 carbon atoms, dodecylbenzyl, octyl-phenoxy-ethoxy-ethyl; R1 alone is selected from the group consisting of alkyl, phenyl, chlorophenyl, bromo-phenyl, alkylphenyl, benzyl, alkylbenzyl, dialkylbenzyl, chlorobenzyl, dichlorobenzyl, dibromobenzyl, naphthyl-lower alkyl, and alkyl-naphthyl-ammonium chloride, in which alkyl it is 8 to 24 carbon atoms; R2 alone is lower alkyl; R3 alone is lower alkyl; R1 together with one of the groups R2 and R3 is selected from the group consisting of morpholino, methylmorpholine and piperidine: and R1, R2 and R3 together are selected from the group consisting of pyridine, quinoline and isoquinoline; A, B, D and F are each selected from the group consisting of hydrogen, lower alkyl, chlorine, bromine, iodine, phenyl, lower alkylphenyl, alkoxy-lower phenyl, chlorophenyl, bromophenyl, benzyl, alkyl. -lower benzyl, lower alkoxy-benzyl, chlorobenzyl and bromobenzyl; G is selected from the group consisting of lower alkyl, chlorine, bromine, iodine, phenyl, lower alkyl-phenyl, lower alkoxy-phenyl, chlorophenyl, bromo-phenyl, benzyl, lower alkyl-benzyl, lower alkoxy-benzyl, chlorobenzyl and bromobenzyl. ; Y is selected from the group consisting of oxygen and sulfur and X is selected from the group consisting of chlorine, bromine and iodine, characterized in that it consists in reacting an alkaline phenate or thiophenate with the quaternary ammonium halide and the chosen halogen. (Machine-translation by Google Translate, not legally binding)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES356174A ES356174A1 (en) | 1968-07-15 | 1968-07-15 | Procedure for obtaining a quaternary ammonium complex. (Machine-translation by Google Translate, not legally binding) |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES356174A ES356174A1 (en) | 1968-07-15 | 1968-07-15 | Procedure for obtaining a quaternary ammonium complex. (Machine-translation by Google Translate, not legally binding) |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES356174A1 true ES356174A1 (en) | 1970-01-01 |
Family
ID=8449754
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES356174A Expired ES356174A1 (en) | 1968-07-15 | 1968-07-15 | Procedure for obtaining a quaternary ammonium complex. (Machine-translation by Google Translate, not legally binding) |
Country Status (1)
| Country | Link |
|---|---|
| ES (1) | ES356174A1 (en) |
-
1968
- 1968-07-15 ES ES356174A patent/ES356174A1/en not_active Expired
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