PL126676B1 - Method for producing 0,0-dimethylphosphodithionate of ethyl mercaptosuccinate - Google Patents
Method for producing 0,0-dimethylphosphodithionate of ethyl mercaptosuccinate Download PDFInfo
- Publication number
- PL126676B1 PL126676B1 PL1981230260A PL23026081A PL126676B1 PL 126676 B1 PL126676 B1 PL 126676B1 PL 1981230260 A PL1981230260 A PL 1981230260A PL 23026081 A PL23026081 A PL 23026081A PL 126676 B1 PL126676 B1 PL 126676B1
- Authority
- PL
- Poland
- Prior art keywords
- acid
- solvent
- amount
- malathion
- dimethyl
- Prior art date
Links
- KLXFSKITMRWDPM-UHFFFAOYSA-N diethyl 2-sulfanylbutanedioate Chemical compound CCOC(=O)CC(S)C(=O)OCC KLXFSKITMRWDPM-UHFFFAOYSA-N 0.000 title claims description 3
- 238000004519 manufacturing process Methods 0.000 title description 5
- 238000000034 method Methods 0.000 claims description 66
- 239000002904 solvent Substances 0.000 claims description 47
- CZGGKXNYNPJFAX-UHFFFAOYSA-N Dimethyldithiophosphate Chemical compound COP(S)(=S)OC CZGGKXNYNPJFAX-UHFFFAOYSA-N 0.000 claims description 41
- 239000005949 Malathion Substances 0.000 claims description 38
- JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 claims description 38
- 229960000453 malathion Drugs 0.000 claims description 38
- 239000002253 acid Substances 0.000 claims description 34
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 claims description 23
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 21
- 238000006243 chemical reaction Methods 0.000 claims description 19
- 238000004821 distillation Methods 0.000 claims description 17
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 239000011541 reaction mixture Substances 0.000 claims description 10
- 238000001704 evaporation Methods 0.000 claims description 9
- 230000008020 evaporation Effects 0.000 claims description 9
- 239000012429 reaction media Substances 0.000 claims description 8
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 7
- 238000009835 boiling Methods 0.000 claims description 6
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 6
- JSJFLHPWPFCJTN-UHFFFAOYSA-N dimethyl phosphono phosphate Chemical compound COP(=O)(OC)OP(O)(O)=O JSJFLHPWPFCJTN-UHFFFAOYSA-N 0.000 claims description 6
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 claims description 6
- 238000000746 purification Methods 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- PXXNTAGJWPJAGM-VCOUNFBDSA-N Decaline Chemical compound C=1([C@@H]2C3)C=C(OC)C(OC)=CC=1OC(C=C1)=CC=C1CCC(=O)O[C@H]3C[C@H]1N2CCCC1 PXXNTAGJWPJAGM-VCOUNFBDSA-N 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 239000012071 phase Substances 0.000 description 11
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 5
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 description 5
- 238000010533 azeotropic distillation Methods 0.000 description 4
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 4
- 238000007701 flash-distillation Methods 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000010908 decantation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- -1 ethyl fumar Chemical compound 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- PLFFHJWXOGYWPR-HEDMGYOXSA-N (4r)-4-[(3r,3as,5ar,5br,7as,11as,11br,13ar,13bs)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]pentan-1-ol Chemical compound C([C@]1(C)[C@H]2CC[C@H]34)CCC(C)(C)[C@@H]1CC[C@@]2(C)[C@]4(C)CC[C@@H]1[C@]3(C)CC[C@@H]1[C@@H](CCCO)C PLFFHJWXOGYWPR-HEDMGYOXSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000001944 continuous distillation Methods 0.000 description 1
- 239000001177 diphosphate Substances 0.000 description 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 1
- RDYMFSUJUZBWLH-UHFFFAOYSA-N endosulfan Chemical compound C12COS(=O)OCC2C2(Cl)C(Cl)=C(Cl)C1(Cl)C2(Cl)Cl RDYMFSUJUZBWLH-UHFFFAOYSA-N 0.000 description 1
- XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/1651—Esters of thiophosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
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)
- Luminescent Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8007243A FR2478644A1 (fr) | 1980-03-21 | 1980-03-21 | Procede de preparation de malathion |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL230260A1 PL230260A1 (index.php) | 1981-11-27 |
| PL126676B1 true PL126676B1 (en) | 1983-08-31 |
Family
ID=9240351
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1981230260A PL126676B1 (en) | 1980-03-21 | 1981-03-20 | Method for producing 0,0-dimethylphosphodithionate of ethyl mercaptosuccinate |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4367180A (index.php) |
| EP (1) | EP0037349B1 (index.php) |
| AU (1) | AU547037B2 (index.php) |
| BR (1) | BR8101680A (index.php) |
| CA (1) | CA1169432A (index.php) |
| DD (1) | DD157804A5 (index.php) |
| DE (1) | DE3160055D1 (index.php) |
| DK (1) | DK126881A (index.php) |
| ES (1) | ES500558A0 (index.php) |
| FR (1) | FR2478644A1 (index.php) |
| HU (1) | HU188284B (index.php) |
| IE (1) | IE51442B1 (index.php) |
| NZ (1) | NZ196554A (index.php) |
| PL (1) | PL126676B1 (index.php) |
| PT (1) | PT72713B (index.php) |
| RO (1) | RO81910A (index.php) |
| SU (1) | SU1060117A3 (index.php) |
| YU (1) | YU66181A (index.php) |
| ZA (1) | ZA811794B (index.php) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6524246B1 (en) * | 2000-10-13 | 2003-02-25 | Sonocine, Inc. | Ultrasonic cellular tissue screening tool |
| US8158139B2 (en) * | 2004-07-12 | 2012-04-17 | Taro Pharmaceuticals North America, Inc. | Topical gel formulation comprising organophosphate insecticide and preparation thereof |
| WO2006017263A1 (en) * | 2004-07-12 | 2006-02-16 | Taro Pharmaceutical Industries Ltd. | Topical gel formulation comprising organophosphate insecticide and its preparation thereof |
| US20060121073A1 (en) * | 2004-07-12 | 2006-06-08 | Sandhya Goyal | Topical gel formulation comprising insecticide and its preparation thereof |
| US7560445B2 (en) * | 2005-07-06 | 2009-07-14 | Taro Pharmaceuticals North America, Inc. | Process for preparing malathion for pharmaceutical use |
| US8138366B2 (en) | 2007-07-09 | 2012-03-20 | Suven Life Sciences Limited | Process for the preparation of malathion and its intermediate |
| ES2477888T3 (es) | 2010-01-20 | 2014-07-18 | W.R. Grace & Co.-Conn. | Retardante del fraguado aplicado a una superficie que induce una alta curación |
| BR112021005898B1 (pt) * | 2018-09-27 | 2023-12-19 | Cheminova A/S | Método de produção de malation |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1427827A (fr) * | 1964-12-08 | 1966-02-11 | Ministerul Ind Petrolului | Procédé de fabrication de dithiophosphate o, o-diméthyl-s-(1, 2-dicarbéthoxyéthylique |
| US3463841A (en) * | 1966-11-01 | 1969-08-26 | American Cyanamid Co | Malathion manufacture |
| FR1541883A (fr) * | 1966-11-01 | 1968-10-11 | American Cyanamid Co | Procédé perfectionné de préparation d'o, o-diméthylphosphorodithioate de mercaptosuccinate de diéthyle |
-
1980
- 1980-03-21 FR FR8007243A patent/FR2478644A1/fr active Granted
-
1981
- 1981-03-11 US US06/242,539 patent/US4367180A/en not_active Expired - Fee Related
- 1981-03-16 YU YU00661/81A patent/YU66181A/xx unknown
- 1981-03-18 NZ NZ196554A patent/NZ196554A/xx unknown
- 1981-03-18 CA CA000373311A patent/CA1169432A/en not_active Expired
- 1981-03-18 AU AU68474/81A patent/AU547037B2/en not_active Ceased
- 1981-03-18 IE IE590/81A patent/IE51442B1/en unknown
- 1981-03-18 ZA ZA00811794A patent/ZA811794B/xx unknown
- 1981-03-18 RO RO81103735A patent/RO81910A/ro unknown
- 1981-03-19 DE DE8181420039T patent/DE3160055D1/de not_active Expired
- 1981-03-19 EP EP81420039A patent/EP0037349B1/fr not_active Expired
- 1981-03-20 DD DD81228498A patent/DD157804A5/de unknown
- 1981-03-20 ES ES500558A patent/ES500558A0/es active Granted
- 1981-03-20 DK DK126881A patent/DK126881A/da not_active Application Discontinuation
- 1981-03-20 PL PL1981230260A patent/PL126676B1/pl unknown
- 1981-03-20 PT PT72713A patent/PT72713B/pt unknown
- 1981-03-20 HU HU81725A patent/HU188284B/hu unknown
- 1981-03-20 BR BR8101680A patent/BR8101680A/pt unknown
- 1981-03-20 SU SU813261996A patent/SU1060117A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| AU6847481A (en) | 1981-09-24 |
| FR2478644B1 (index.php) | 1984-06-08 |
| EP0037349B1 (fr) | 1983-02-09 |
| AU547037B2 (en) | 1985-10-03 |
| BR8101680A (pt) | 1981-09-22 |
| YU66181A (en) | 1983-12-31 |
| US4367180A (en) | 1983-01-04 |
| CA1169432A (en) | 1984-06-19 |
| DE3160055D1 (en) | 1983-03-17 |
| IE51442B1 (en) | 1986-12-24 |
| ZA811794B (en) | 1982-03-31 |
| IE810590L (en) | 1981-09-21 |
| PL230260A1 (index.php) | 1981-11-27 |
| ES8205415A1 (es) | 1982-01-01 |
| DK126881A (da) | 1981-09-22 |
| SU1060117A3 (ru) | 1983-12-07 |
| HU188284B (en) | 1986-03-28 |
| PT72713B (fr) | 1982-11-15 |
| DD157804A5 (de) | 1982-12-08 |
| NZ196554A (en) | 1983-06-17 |
| PT72713A (fr) | 1981-04-01 |
| RO81910B (ro) | 1983-09-30 |
| FR2478644A1 (fr) | 1981-09-25 |
| EP0037349A1 (fr) | 1981-10-07 |
| ES500558A0 (es) | 1982-01-01 |
| RO81910A (ro) | 1983-10-15 |
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