GB779449A - New organic phosphorus-containing derivative, process for its preparation and compositions containing it - Google Patents
New organic phosphorus-containing derivative, process for its preparation and compositions containing itInfo
- Publication number
- GB779449A GB779449A GB1258856A GB1258856A GB779449A GB 779449 A GB779449 A GB 779449A GB 1258856 A GB1258856 A GB 1258856A GB 1258856 A GB1258856 A GB 1258856A GB 779449 A GB779449 A GB 779449A
- Authority
- GB
- United Kingdom
- Prior art keywords
- solution
- pyrone
- methoxy
- sodium
- yield
- 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
- 239000000203 mixture Substances 0.000 title abstract 8
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title 1
- 229910052698 phosphorus Inorganic materials 0.000 title 1
- 239000011574 phosphorus Substances 0.000 title 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 9
- 239000000243 solution Substances 0.000 abstract 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 4
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 abstract 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 3
- 239000005864 Sulphur Substances 0.000 abstract 3
- 239000002270 dispersing agent Substances 0.000 abstract 3
- 235000019441 ethanol Nutrition 0.000 abstract 3
- 239000002917 insecticide Substances 0.000 abstract 3
- 150000003017 phosphorus Chemical class 0.000 abstract 3
- 229910052708 sodium Inorganic materials 0.000 abstract 3
- 239000011734 sodium Substances 0.000 abstract 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 abstract 3
- 230000009885 systemic effect Effects 0.000 abstract 3
- MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 abstract 2
- 238000009835 boiling Methods 0.000 abstract 2
- CZHYKKAKFWLGJO-UHFFFAOYSA-N dimethyl phosphite Chemical compound COP([O-])OC CZHYKKAKFWLGJO-UHFFFAOYSA-N 0.000 abstract 2
- 239000003995 emulsifying agent Substances 0.000 abstract 2
- 239000000839 emulsion Substances 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- 239000000725 suspension Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 abstract 1
- ZZYXUGFBXVXINX-UHFFFAOYSA-N 2-(chloromethyl)-5-methoxypyran-4-one Chemical compound COC1=COC(CCl)=CC1=O ZZYXUGFBXVXINX-UHFFFAOYSA-N 0.000 abstract 1
- 239000005995 Aluminium silicate Substances 0.000 abstract 1
- RVTVTGRRXQKTHB-UHFFFAOYSA-N C1(=CC=C(C=C1)S(=O)(=O)O)C.OCC=1OC=C(C(C1)=O)OC Chemical compound C1(=CC=C(C=C1)S(=O)(=O)O)C.OCC=1OC=C(C(C1)=O)OC RVTVTGRRXQKTHB-UHFFFAOYSA-N 0.000 abstract 1
- 241000488583 Panonychus ulmi Species 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 1
- 230000000895 acaricidal effect Effects 0.000 abstract 1
- 239000000642 acaricide Substances 0.000 abstract 1
- 239000013543 active substance Substances 0.000 abstract 1
- 239000000443 aerosol Substances 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 235000012211 aluminium silicate Nutrition 0.000 abstract 1
- 239000003610 charcoal Substances 0.000 abstract 1
- 229940125782 compound 2 Drugs 0.000 abstract 1
- 239000012141 concentrate Substances 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- 230000003226 decolorizating effect Effects 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 238000010790 dilution Methods 0.000 abstract 1
- 239000012895 dilution Substances 0.000 abstract 1
- 125000004185 ester group Chemical group 0.000 abstract 1
- 238000001914 filtration Methods 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 239000003701 inert diluent Substances 0.000 abstract 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052753 mercury Inorganic materials 0.000 abstract 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 230000000361 pesticidal effect Effects 0.000 abstract 1
- 239000000575 pesticide Substances 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- 235000009518 sodium iodide Nutrition 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
- 230000002195 synergetic effect Effects 0.000 abstract 1
- 239000000454 talc Substances 0.000 abstract 1
- 229910052623 talc Inorganic materials 0.000 abstract 1
- 239000000080 wetting agent Substances 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/6552—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a six-membered ring
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)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention comprises as a new product: 2-(0,0 - dimethylthiolophosphorylmethyl) - 5 - methoxy-4-pyrone of the formula <FORM:0779449/IV(b)/1> It may be obtained by reacting a salt of the general formula (CH3O)2P(O).S.Me where Me represents an alkali metal such as sodium or potassium with a derivative of g -pyrone of the general formula <FORM:0779449/IV(b)/2> where Z represents a halogen atom or a reactive ester group such as a sulphate or sulphonate group. The reaction is preferably effected in an organic solvent such as an aliphatic alcohol or ketone and it is preferred to employ a reaction temperature of 50 DEG to 100 DEG C. and more preferably at about the boiling point of the solvent employed. In examples: (1) a solution of sodium methylate in methyl alcohol is added dropwise to a suspension prepared from benzene, sulphur, and dimethylphosphite, the temperature being kept below 5 DEG C. The residual sulphur is filtered off and the solution added dropwise to a mixture prepared from 2-chloromethyl - 5 - methoxy - 4 - pyrone, sodium iodide and methyl ethyl ketone. The mixture is allowed to stand overnight at room temperature, filtered to remove the salt formed and concentrated under a pressure of 20 to 30 mm. Hg at 40-50 DEG C. to yield a viscous liquid which crystallizes on cooling to yield a solid which is purified by dissolving in boiling benzene and treating with decolourising charcoal to yield the 2 - (0,0 - dimethylthiolophosphorylmethyl)-5-methoxy-4-pyrone; (2) the same product is obtained by reacting sodium 0,0-dimethylthionophosphate with 2-hydroxymethyl-5-methoxy-4-pyrone p-toluene sulphonate in methyl ethyl ketone, the sodium 0,0-dimethylthionophosphate being obtained by adding a solution of sodium methylate in methyl alcohol at about 0 DEG to 5 DEG C. to a suspension of dimethylphosphite, methyl alcohol, and flowers of sulphur, filtering off the residual sulphur and then concentrating the solution at 45 DEG C. under a pressure of 20-30 mm. mercury. The product is effective as a pesticide and systemic insecticide (see Group VI).ALSO:A pesticidal composition comprises the compound 2 - (O, O - dimethylthidophoxylmethyl) - 5 - methoxy - 4 - pyrone of the formula: <FORM:0779449/VI/1> (see Group IV(b)) together with an inert diluent. The diluent may be a solid such as talc or kaolin or the composition may be in the form of an aerosol, emulsion or solution in water or in an organic or aqueous organic medium. The emulsion or solution may contain a wetting agent, dispersing agent or emulsifier of the ionic or non-ionic type and the phosphorus derivative may be formulated as a self-emulsifying concentrate containing the active substance dissolved in the dispersing agent or in a solvent compatible with and containing the dispersing agent, the composition being made ready for use by adding water. Other insecticides including substances having a synergistic effect may be included in the compositions. In examples: (1) the phosphorus derivative is dissolved in a mixture of ethyl alcohol and acetone and a non-ionic emulsifying agent and terpinolene are added followed by the addition of ethyl alcohol to yield a solution containing 10 gm. of active product per 100 cc. which is used after appropriate dilution to combat aphides and red spiders; (2) as in (1) except that the ethyl alcohol is repaced by acetone. The phosphorus derivative is stated to be especially effective as a systemic insecticide and systemic acaricide and examples are given to show its effectiveness as such.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1258856A GB779449A (en) | 1956-04-24 | 1956-04-24 | New organic phosphorus-containing derivative, process for its preparation and compositions containing it |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1258856A GB779449A (en) | 1956-04-24 | 1956-04-24 | New organic phosphorus-containing derivative, process for its preparation and compositions containing it |
Publications (1)
Publication Number | Publication Date |
---|---|
GB779449A true GB779449A (en) | 1957-07-17 |
Family
ID=10007413
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1258856A Expired GB779449A (en) | 1956-04-24 | 1956-04-24 | New organic phosphorus-containing derivative, process for its preparation and compositions containing it |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB779449A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1116217B (en) * | 1958-06-04 | 1961-11-02 | Sandoz Ag | Process for the preparation of thiophosphoric acid esters |
-
1956
- 1956-04-24 GB GB1258856A patent/GB779449A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1116217B (en) * | 1958-06-04 | 1961-11-02 | Sandoz Ag | Process for the preparation of thiophosphoric acid esters |
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