DE1160436B - Verfahren zur Herstellung von Phosphorsaeureestern, -esteramiden bzw. -esterdiamiden - Google Patents
Verfahren zur Herstellung von Phosphorsaeureestern, -esteramiden bzw. -esterdiamidenInfo
- Publication number
- DE1160436B DE1160436B DEF36280A DEF0036280A DE1160436B DE 1160436 B DE1160436 B DE 1160436B DE F36280 A DEF36280 A DE F36280A DE F0036280 A DEF0036280 A DE F0036280A DE 1160436 B DE1160436 B DE 1160436B
- Authority
- DE
- Germany
- Prior art keywords
- phosphoric acid
- alkyl
- ester
- ammonia
- general formula
- 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.)
- Pending
Links
- -1 ester amides Chemical class 0.000 title claims description 22
- 238000000034 method Methods 0.000 title claims description 12
- 150000003014 phosphoric acid esters Chemical class 0.000 title claims description 6
- 238000004519 manufacturing process Methods 0.000 title claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 10
- 230000000694 effects Effects 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 9
- 229910021529 ammonia Inorganic materials 0.000 claims description 6
- 241000607479 Yersinia pestis Species 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 5
- 239000011230 binding agent Substances 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000005265 dialkylamine group Chemical group 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 3
- 239000013067 intermediate product Substances 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 150000004707 phenolate Chemical class 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 241000238631 Hexapoda Species 0.000 claims 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 239000000243 solution Substances 0.000 description 15
- 241001454295 Tetranychidae Species 0.000 description 10
- 241001124076 Aphididae Species 0.000 description 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 230000001988 toxicity Effects 0.000 description 7
- 231100000419 toxicity Toxicity 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 230000009885 systemic effect Effects 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- 241000256602 Isoptera Species 0.000 description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 241000238876 Acari Species 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000255925 Diptera Species 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 241000118205 Ovicides Species 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- JGFZITGNFAVSKU-UHFFFAOYSA-N 3,5-dimethyl-4-(methylsulfanyl)phenol Chemical compound CSC1=C(C)C=C(O)C=C1C JGFZITGNFAVSKU-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- 241001425390 Aphis fabae Species 0.000 description 1
- 241000255581 Drosophila <fruit fly, genus> Species 0.000 description 1
- 241000122098 Ephestia kuehniella Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241001454293 Tetranychus urticae Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000027455 binding Effects 0.000 description 1
- 238000009739 binding Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 244000078703 ectoparasite Species 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- OYQVKYFWJZYYOA-UHFFFAOYSA-N methylamino dihydrogen phosphate Chemical compound CNOP(O)(O)=O OYQVKYFWJZYYOA-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 231100000194 ovacidal Toxicity 0.000 description 1
- 230000003151 ovacidal effect Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007858 starting material Substances 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
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/12—Esters of phosphoric acids with hydroxyaryl compounds
-
- 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
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2404—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/242—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic of hydroxyaryl 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)
- Fertilizers (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL137339D NL137339C (US06824948-20041130-C00056.png) | 1962-03-15 | ||
| NL289967D NL289967A (US06824948-20041130-C00056.png) | 1962-03-15 | ||
| BE629625D BE629625A (US06824948-20041130-C00056.png) | 1962-03-15 | ||
| DEF36280A DE1160436B (de) | 1962-03-15 | 1962-03-15 | Verfahren zur Herstellung von Phosphorsaeureestern, -esteramiden bzw. -esterdiamiden |
| CH262863A CH430319A (de) | 1962-03-15 | 1963-03-01 | Schädlingsbekämpfungsmittel |
| US264716A US3294875A (en) | 1962-03-15 | 1963-03-12 | Phosphoric acid esters, ester amides or ester diamides |
| DK115963AA DK107396C (da) | 1962-03-15 | 1963-03-13 | Middel til bekæmpelse af skadelige organismer og fremgangsmåde til fremstilling af phosphorsyreestere, -esteramider eller -esterdiamider til anvendelse i midlet. |
| FR927859A FR1351765A (fr) | 1962-03-15 | 1963-03-13 | Parasiticides agricoles et leur procédé de préparation |
| GB10146/63A GB975354A (en) | 1962-03-15 | 1963-03-14 | Alkylmercaptoaryl phosphorus-containing esters |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF36280A DE1160436B (de) | 1962-03-15 | 1962-03-15 | Verfahren zur Herstellung von Phosphorsaeureestern, -esteramiden bzw. -esterdiamiden |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1160436B true DE1160436B (de) | 1964-01-02 |
Family
ID=7096375
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF36280A Pending DE1160436B (de) | 1962-03-15 | 1962-03-15 | Verfahren zur Herstellung von Phosphorsaeureestern, -esteramiden bzw. -esterdiamiden |
Country Status (7)
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1075609B (de) * | 1956-04-02 | 1960-02-18 | The Dow Chemical Company, Midland Mich (V St A) | Verfahren zur Herstellung neuer O - Aryl O - methylthiophosphorsaureamidester |
| US2929762A (en) * | 1958-07-22 | 1960-03-22 | Dow Chemical Co | Phosphoramidates |
| AT213903B (de) * | 1958-03-08 | 1961-03-10 | Bayer Ag | Verfahren zur Herstellung neuer Alkylmercapto-phenyl-phosphorsäure- bzw.-thionophosphorsäure-esteramide bzw.-diamide |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE556009A (US06824948-20041130-C00056.png) * | 1956-03-22 | |||
| DE1089376B (de) * | 1958-02-12 | 1960-09-22 | Bayer Ag | Verfahren zur Herstellung von Thiophosphorsaeureestern bzw. Thiophosphonsaeureestern |
| US2978479A (en) * | 1958-03-08 | 1961-04-04 | Bayer Ag | Pest control agents |
| US3092544A (en) * | 1961-11-03 | 1963-06-04 | Dow Chemical Co | Organo phosphorous nematocide |
-
0
- BE BE629625D patent/BE629625A/xx unknown
- NL NL289967D patent/NL289967A/xx unknown
- NL NL137339D patent/NL137339C/xx active
-
1962
- 1962-03-15 DE DEF36280A patent/DE1160436B/de active Pending
-
1963
- 1963-03-01 CH CH262863A patent/CH430319A/de unknown
- 1963-03-12 US US264716A patent/US3294875A/en not_active Expired - Lifetime
- 1963-03-13 DK DK115963AA patent/DK107396C/da active
- 1963-03-14 GB GB10146/63A patent/GB975354A/en not_active Expired
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1075609B (de) * | 1956-04-02 | 1960-02-18 | The Dow Chemical Company, Midland Mich (V St A) | Verfahren zur Herstellung neuer O - Aryl O - methylthiophosphorsaureamidester |
| AT213903B (de) * | 1958-03-08 | 1961-03-10 | Bayer Ag | Verfahren zur Herstellung neuer Alkylmercapto-phenyl-phosphorsäure- bzw.-thionophosphorsäure-esteramide bzw.-diamide |
| US2929762A (en) * | 1958-07-22 | 1960-03-22 | Dow Chemical Co | Phosphoramidates |
Also Published As
| Publication number | Publication date |
|---|---|
| US3294875A (en) | 1966-12-27 |
| NL289967A (US06824948-20041130-C00056.png) | |
| CH430319A (de) | 1967-02-15 |
| BE629625A (US06824948-20041130-C00056.png) | |
| GB975354A (en) | 1964-11-18 |
| NL137339C (US06824948-20041130-C00056.png) | |
| DK107396C (da) | 1967-05-22 |
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