GB1161201A - Improvements in or relating to the Production of Quaternary Phosphonium Compounds. - Google Patents
Improvements in or relating to the Production of Quaternary Phosphonium Compounds.Info
- Publication number
- GB1161201A GB1161201A GB31287/65A GB3128765A GB1161201A GB 1161201 A GB1161201 A GB 1161201A GB 31287/65 A GB31287/65 A GB 31287/65A GB 3128765 A GB3128765 A GB 3128765A GB 1161201 A GB1161201 A GB 1161201A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- tetrahydro
- dimethoxy
- alkyl
- phosphonium salts
- 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
- 150000004023 quaternary phosphonium compounds Chemical class 0.000 title 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
- -1 pyrrolidino, morpholino, piperidino Chemical group 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 150000004714 phosphonium salts Chemical class 0.000 abstract 3
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- 230000002378 acidificating effect Effects 0.000 abstract 2
- 150000001768 cations Chemical class 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- KMXSGVJFXNVELP-UHFFFAOYSA-N 2-[1-[3-(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)-2-oxopropyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]ethyl-triphenylphosphanium Chemical class COC=1C=C2CCN(C(C2=CC=1OC)CC(CC1NCCC2=CC(=C(C=C12)OC)OC)=O)CC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1 KMXSGVJFXNVELP-UHFFFAOYSA-N 0.000 abstract 1
- XDWAYICEXWBZBO-UHFFFAOYSA-N 2-morpholin-4-ylethyl(triphenyl)phosphanium Chemical class C1COCCN1CC[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 XDWAYICEXWBZBO-UHFFFAOYSA-N 0.000 abstract 1
- GDLBZWYJICEYQC-UHFFFAOYSA-N 9,10-dimethoxy-2-methyl-4,6,7,11b-tetrahydro-1H-benzo[a]quinolizine Chemical compound COC1=CC2=C(C3CC(=CCN3CC2)C)C=C1OC GDLBZWYJICEYQC-UHFFFAOYSA-N 0.000 abstract 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 abstract 1
- ATTZFSUZZUNHBP-UHFFFAOYSA-N Piperonyl sulfoxide Chemical compound CCCCCCCCS(=O)C(C)CC1=CC=C2OCOC2=C1 ATTZFSUZZUNHBP-UHFFFAOYSA-N 0.000 abstract 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 125000000129 anionic group Chemical group 0.000 abstract 1
- 150000003842 bromide salts Chemical class 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 abstract 1
- 239000012259 ether extract Substances 0.000 abstract 1
- GELSOTNVVKOYAW-UHFFFAOYSA-N ethyl(triphenyl)phosphanium Chemical class C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 GELSOTNVVKOYAW-UHFFFAOYSA-N 0.000 abstract 1
- 239000000284 extract Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229940075930 picrate Drugs 0.000 abstract 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-M picrate anion Chemical compound [O-]C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-M 0.000 abstract 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 abstract 1
- 239000002798 polar solvent Substances 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 150000003335 secondary amines Chemical class 0.000 abstract 1
- 229910000104 sodium hydride Inorganic materials 0.000 abstract 1
- 239000012312 sodium hydride Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical class C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/54—Quaternary phosphonium compounds
- C07F9/5407—Acyclic saturated phosphonium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Hydrogenated Pyridines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Fireproofing Substances (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB31287/65A GB1161201A (en) | 1965-10-22 | 1965-10-22 | Improvements in or relating to the Production of Quaternary Phosphonium Compounds. |
| DK533566AA DK122889B (da) | 1965-10-22 | 1966-10-14 | Fremgangsmåde til fremstilling af phosphoniumforbindelser. |
| US587394A US3560494A (en) | 1965-10-22 | 1966-10-18 | Process for phosphonic ethylation of amines |
| CH1521466A CH473838A (de) | 1965-10-22 | 1966-10-20 | Verfahren zur Herstellung von Phosphoniumverbindungen |
| BE688729D BE688729A (US08197722-20120612-C00042.png) | 1965-10-22 | 1966-10-21 | |
| DE19661620737 DE1620737C3 (de) | 1965-10-22 | 1966-10-21 | Verfahren zur Herstellung von substituierten Äthylphosphoniumsalzen |
| ES0332544A ES332544A1 (es) | 1965-10-22 | 1966-10-21 | Un metodo para la preparacion de un compuesto que contiene cation aminoetilfosfonio. |
| FR81217A FR1504685A (US08197722-20120612-C00042.png) | 1965-10-22 | 1966-10-22 | |
| NL6615818A NL6615818A (US08197722-20120612-C00042.png) | 1965-10-22 | 1966-11-09 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB31287/65A GB1161201A (en) | 1965-10-22 | 1965-10-22 | Improvements in or relating to the Production of Quaternary Phosphonium Compounds. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1161201A true GB1161201A (en) | 1969-08-13 |
Family
ID=10320886
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB31287/65A Expired GB1161201A (en) | 1965-10-22 | 1965-10-22 | Improvements in or relating to the Production of Quaternary Phosphonium Compounds. |
Country Status (8)
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019023798A1 (en) * | 2017-07-31 | 2019-02-07 | Exigence Technologies Inc. | POLYMERIZABLE COMPOUNDS HAVING ONE OR MORE SURFACE-TYPE PROPERTIES |
-
1965
- 1965-10-22 GB GB31287/65A patent/GB1161201A/en not_active Expired
-
1966
- 1966-10-14 DK DK533566AA patent/DK122889B/da unknown
- 1966-10-18 US US587394A patent/US3560494A/en not_active Expired - Lifetime
- 1966-10-20 CH CH1521466A patent/CH473838A/de not_active IP Right Cessation
- 1966-10-21 BE BE688729D patent/BE688729A/xx unknown
- 1966-10-21 ES ES0332544A patent/ES332544A1/es not_active Expired
- 1966-10-22 FR FR81217A patent/FR1504685A/fr not_active Expired
- 1966-11-09 NL NL6615818A patent/NL6615818A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE1620737B2 (de) | 1975-08-21 |
| DK122889B (da) | 1972-04-24 |
| NL6615818A (US08197722-20120612-C00042.png) | 1968-05-10 |
| DE1620737A1 (de) | 1970-09-03 |
| ES332544A1 (es) | 1967-08-01 |
| FR1504685A (US08197722-20120612-C00042.png) | 1968-02-14 |
| CH473838A (de) | 1969-06-15 |
| US3560494A (en) | 1971-02-02 |
| BE688729A (US08197722-20120612-C00042.png) | 1967-04-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES411804A1 (es) | Procedimiento para la obtencion de derivados de quinoxalinay quinazolina. | |
| GB1161201A (en) | Improvements in or relating to the Production of Quaternary Phosphonium Compounds. | |
| GB1264485A (US08197722-20120612-C00042.png) | ||
| US2652398A (en) | N-substituted-2-amino (methyl) quinolines | |
| US3381013A (en) | Heterocyclicamino ethers of benzylphenols | |
| Shapiro et al. | Guanamine diuretics | |
| DK188183A (da) | Thiomethylpyridinderivater, fremgangsmaade til deres fremstilling og laegemidler indeholdende disse forbindelser | |
| ES320729A1 (es) | Procedimiento para la sintesis de nuevos derivados de acido antranilico. | |
| US3755334A (en) | New quaternization method | |
| GB907646A (en) | Method of production of new derivatives of diazepin | |
| GB1268196A (en) | Pyridine derivatives and their manufacture | |
| US2561948A (en) | Aminoalkylated diamino diphenyl sulfones | |
| GB1381755A (en) | Substituted n-alkylamino-acrylamides | |
| GB1131467A (en) | New basic derivatives of benzoxazine and methods for their production | |
| GB1102891A (en) | Process for the preparation of heterocyclammonium betaines | |
| GB625347A (en) | Methin dyes containing an isoquinoline nucleus and photographic emulsions containing them | |
| GB1079216A (en) | Ylenals and process for their production | |
| GB778808A (en) | Azacyclic compounds and process for making them | |
| GB1126669A (en) | Process for production of basically substituted phthalazones | |
| ES294533A1 (es) | Procedimiento para la producciën de nuevos compuestos heterociclicos | |
| ES354083A1 (es) | Un procedimiento para la obtencion de 1 - fenoxi-2-hidroxi-3-butilaminopropanos. | |
| Work | 80. The synthesis of amines from amides through the amidodichlorides | |
| GB1026155A (en) | Diheterocyclic mono-azo compounds and methods for their production | |
| Kochkanyan et al. | Synthesis and peculiarities of the structures of betaine aldehydes with polynuclear heteroaromatic cations | |
| ES340648A2 (es) | Un procedimiento para la obtencion de nuevas 2-amino-halo- geno-benzilaminas. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |