HU184823B - Process for preparing s-alkyl-phosphono-dithionic acid halogenides with brandhed chains - Google Patents
Process for preparing s-alkyl-phosphono-dithionic acid halogenides with brandhed chains Download PDFInfo
- Publication number
- HU184823B HU184823B HU802142A HU214280A HU184823B HU 184823 B HU184823 B HU 184823B HU 802142 A HU802142 A HU 802142A HU 214280 A HU214280 A HU 214280A HU 184823 B HU184823 B HU 184823B
- Authority
- HU
- Hungary
- Prior art keywords
- alkyl
- formula
- compound
- preparation
- solvent
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 25
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 11
- 238000006243 chemical reaction Methods 0.000 claims abstract description 9
- 238000002360 preparation method Methods 0.000 claims abstract description 9
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 4
- 125000005843 halogen group Chemical group 0.000 claims abstract description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 11
- 239000002904 solvent Substances 0.000 claims description 10
- 239000011541 reaction mixture Substances 0.000 claims description 6
- 150000003512 tertiary amines Chemical class 0.000 claims description 4
- 239000003153 chemical reaction reagent Substances 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 150000001356 alkyl thiols Chemical class 0.000 abstract description 3
- 239000002917 insecticide Substances 0.000 abstract description 3
- 239000000543 intermediate Substances 0.000 abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 230000001069 nematicidal effect Effects 0.000 abstract 1
- 239000005645 nematicide Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- -1 phosphonodithiochlorides Chemical class 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 150000003573 thiols Chemical class 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 241000209149 Zea Species 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 230000000507 anthelmentic effect Effects 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- WMXCDAVJEZZYLT-UHFFFAOYSA-N tert-butylthiol Chemical compound CC(C)(C)S WMXCDAVJEZZYLT-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 229940124339 anthelmintic agent Drugs 0.000 description 1
- 239000000921 anthelmintic agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- TUNCWCIKOHOGJX-UHFFFAOYSA-N dichloro-methyl-sulfanylidene-$l^{5}-phosphane Chemical compound CP(Cl)(Cl)=S TUNCWCIKOHOGJX-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 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
-
- 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
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/42—Halides thereof
- C07F9/425—Acid or estermonohalides thereof, e.g. RP(=X)(YR)(Hal) (X, Y = O, S; R = H, or hydrocarbon group)
-
- 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
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7146579A | 1979-08-31 | 1979-08-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU184823B true HU184823B (en) | 1984-10-29 |
Family
ID=22101507
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU802142A HU184823B (en) | 1979-08-31 | 1980-08-29 | Process for preparing s-alkyl-phosphono-dithionic acid halogenides with brandhed chains |
Country Status (15)
| Country | Link |
|---|---|
| EP (1) | EP0025270B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JPS5645494A (cg-RX-API-DMAC7.html) |
| KR (1) | KR830002057B1 (cg-RX-API-DMAC7.html) |
| AT (1) | ATE8634T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU541928B2 (cg-RX-API-DMAC7.html) |
| BR (1) | BR8005509A (cg-RX-API-DMAC7.html) |
| CA (1) | CA1178294A (cg-RX-API-DMAC7.html) |
| DD (1) | DD153846A5 (cg-RX-API-DMAC7.html) |
| DE (1) | DE3068679D1 (cg-RX-API-DMAC7.html) |
| DK (1) | DK369980A (cg-RX-API-DMAC7.html) |
| EG (1) | EG14458A (cg-RX-API-DMAC7.html) |
| ES (1) | ES8105743A1 (cg-RX-API-DMAC7.html) |
| HU (1) | HU184823B (cg-RX-API-DMAC7.html) |
| IL (1) | IL60893A (cg-RX-API-DMAC7.html) |
| ZA (1) | ZA805027B (cg-RX-API-DMAC7.html) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4391760A (en) * | 1980-12-31 | 1983-07-05 | Rhone-Poulenc Agrochimie | S-(Tertiary alkyl) alkylphosphonothioic halides |
| FR2523584B1 (fr) * | 1982-03-17 | 1985-06-28 | Rhone Poulenc Agrochimie | Halogenures d'acides s-(tertioalcoyl) alcoylphosphonothioiques, leur preparation et leur utilisation |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1104506B (de) * | 1959-09-08 | 1961-04-13 | Bayer Ag | Verfahren zur Herstellung von Dithiophosphonsaeureesterfluoriden oder -aziden |
| DE2652922A1 (de) * | 1976-11-20 | 1978-05-24 | Bayer Ag | Diothiophosphonsaeureesterhalogenide, verfahren zu ihrer herstellung und ihre verwendung als zwischenprodukte |
| DE2702049A1 (de) * | 1977-01-19 | 1978-07-20 | Bayer Ag | Substituierte dithiophosphonsaeureesteramide, verfahren zu ihrer herstellung und ihre verwendung als insektizide, akarizide und nematizide |
| DE2714771C2 (de) * | 1977-04-02 | 1984-12-06 | Bayer Ag, 5090 Leverkusen | O-Phenyldithiophosphonsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide, Akarizide und Nematizide |
-
1980
- 1980-08-04 DE DE8080302649T patent/DE3068679D1/de not_active Expired
- 1980-08-04 AT AT80302649T patent/ATE8634T1/de not_active IP Right Cessation
- 1980-08-04 EP EP80302649A patent/EP0025270B1/en not_active Expired
- 1980-08-06 CA CA000357727A patent/CA1178294A/en not_active Expired
- 1980-08-15 ZA ZA00805027A patent/ZA805027B/xx unknown
- 1980-08-15 AU AU61495/80A patent/AU541928B2/en not_active Ceased
- 1980-08-21 IL IL60893A patent/IL60893A/xx unknown
- 1980-08-27 EG EG529/80A patent/EG14458A/xx active
- 1980-08-27 KR KR1019800003398A patent/KR830002057B1/ko not_active Expired
- 1980-08-29 DD DD80223617A patent/DD153846A5/de unknown
- 1980-08-29 HU HU802142A patent/HU184823B/hu not_active IP Right Cessation
- 1980-08-29 ES ES494630A patent/ES8105743A1/es not_active Expired
- 1980-08-29 DK DK369980A patent/DK369980A/da not_active Application Discontinuation
- 1980-08-29 BR BR8005509A patent/BR8005509A/pt unknown
- 1980-09-01 JP JP12099980A patent/JPS5645494A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5645494A (en) | 1981-04-25 |
| ES494630A0 (es) | 1981-06-16 |
| DD153846A5 (de) | 1982-02-03 |
| KR830002057B1 (ko) | 1983-10-08 |
| EG14458A (en) | 1984-06-30 |
| IL60893A0 (en) | 1980-10-26 |
| DE3068679D1 (en) | 1984-08-30 |
| IL60893A (en) | 1984-05-31 |
| AU541928B2 (en) | 1985-01-31 |
| ES8105743A1 (es) | 1981-06-16 |
| KR830003507A (ko) | 1983-06-21 |
| ZA805027B (en) | 1981-08-26 |
| CA1178294A (en) | 1984-11-20 |
| JPS6353197B2 (cg-RX-API-DMAC7.html) | 1988-10-21 |
| AU6149580A (en) | 1981-03-05 |
| DK369980A (da) | 1981-03-01 |
| ATE8634T1 (de) | 1984-08-15 |
| BR8005509A (pt) | 1981-03-10 |
| EP0025270A1 (en) | 1981-03-18 |
| EP0025270B1 (en) | 1984-07-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HU90 | Patent valid on 900628 | ||
| HMM4 | Cancellation of final prot. due to non-payment of fee |