DEF0016110MA - - Google Patents
Info
- Publication number
- DEF0016110MA DEF0016110MA DEF0016110MA DE F0016110M A DEF0016110M A DE F0016110MA DE F0016110M A DEF0016110M A DE F0016110MA
- Authority
- DE
- Germany
- Prior art keywords
- ethyleneimine
- general formula
- derivatives
- carbon tetrachloride
- ecm
- 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.)
- Active
Links
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical class C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 claims description 14
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 239000011230 binding agent Substances 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- -1 amine sulfene halides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DEF0016110MA (enrdf_load_stackoverflow) | ||
DE948330C (de) | Verfahren zur Herstellung von Derivaten des AEthylenimins | |
DE4102337C2 (de) | Verfahren zur Herstellung von Zink-bis-(dibenzyldithiocarbamat) und dessen Derivate | |
EP0158012A1 (de) | Imidazoazolacrabonylverbindungen und ihre Verwendung als Zwischenprodukte für die Herstellung von Arzneimittel | |
DE1154477B (de) | Verfahren zur Herstellung von Nitro- oder Nitritogruppen enthaltenden Silanen | |
DE941193C (de) | Verfahren zur Herstellung von neuen, bisquaternaeren Phosphoniumverbindungen | |
DE1227449B (de) | Verfahren zur Herstellung von Phosphorsaeureestern | |
DE1445659C (de) | Pyndylphosphorverbindungen und Verfahren zu ihrer Herstellung | |
DE2141765A1 (de) | 4-chlor-4-thiazolin-2-one und verfahren zu deren herstellung | |
CH513848A (de) | Verfahren zur Herstellung von Pyrrolinverbindungen | |
EP0113030A1 (de) | Cycloalkenylderivate, ihre Herstellung und Verwendung | |
DE1198360B (de) | Verfahren zur Herstellung von o-Alkyl-S-(l-phenyl-2-alkoxycarbonyl-äthyl) - alkylthiophosphonaten | |
DE1914496C3 (de) | Verfahren zur Herstellung von 1,2,5 -Thiadiazolderivaten | |
DE1167587B (de) | Insektizides Mittel | |
DE593192C (de) | Verfahren zur Darstellung von N-substituierten heterocyclischen Verbindungen | |
DE2660902C2 (de) | Dicarbonsäure-bis[3,5-bis(chlorcarbonyl)-2,4,6-trijodanilid]- Verbindungen und deren Herstellung | |
AT235859B (de) | Verfahren zur Herstellung von neuen, beispielsweise zur Schädlingsbekämpfung verwendbaren Phosphonsäureestern | |
DE1000381C2 (de) | Verfahren zur Herstellung von 2-Thio-3, 3-dialkyl- bzw. 2-Thio-3, 3-dialkenyl-4-oxo-1, 2, 3, 4-tetrahydro-pyridinen | |
DE3150981A1 (de) | 3-amino-2-oxo-thiazol-5-carbonsaeure-derivate und ihre herstellung | |
DE952084C (de) | Verfahren zur Herstellung von organischen Isothiocyanaten | |
DE907298C (de) | Verfahren zur Herstellung von analgetisch wirkenden Verbindungen | |
DE1206903B (de) | Verfahren zur Herstellung von Thiol- bzw. Thionothiolphosphor-(-phosphon)saeureestern | |
DE1183081B (de) | Verfahren zur Herstellung von Thiol- bzw. Thionothiolphosphonsaeureestern | |
DE1136693B (de) | Verfahren zur Herstellung von basisch substituierten Thiolcarbaminsaeure-alkylestern | |
DE1141990B (de) | Verfahren zur Herstellung von Thiophosphinsaeureestern |