SU93341A1 - - Google Patents
Info
- Publication number
- SU93341A1 SU93341A1 SU93341A1 SU 93341 A1 SU93341 A1 SU 93341A1 SU 93341 A1 SU93341 A1 SU 93341A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- alcohol
- solution
- dye
- heated
- ethyl
- Prior art date
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 83
- 235000019441 ethanol Nutrition 0.000 description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 21
- 239000000975 dye Substances 0.000 description 21
- 239000000243 solution Substances 0.000 description 21
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
- 238000010521 absorption reaction Methods 0.000 description 12
- 238000009835 boiling Methods 0.000 description 12
- 239000002244 precipitate Substances 0.000 description 11
- -1 iodoethyl Chemical group 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 238000002425 crystallisation Methods 0.000 description 6
- 230000008025 crystallization Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- JKLNYGDWYRKFKR-UHFFFAOYSA-N ethyl methyl sulfate Chemical compound CCOS(=O)(=O)OC JKLNYGDWYRKFKR-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 3
- 150000003839 salts Chemical group 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 2
- 235000005811 Viola adunca Nutrition 0.000 description 2
- 240000009038 Viola odorata Species 0.000 description 2
- 235000013487 Viola odorata Nutrition 0.000 description 2
- 235000002254 Viola papilionacea Nutrition 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 239000000298 carbocyanine Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- QWYZFXLSWMXLDM-UHFFFAOYSA-M pinacyanol iodide Chemical compound [I-].C1=CC2=CC=CC=C2N(CC)C1=CC=CC1=CC=C(C=CC=C2)C2=[N+]1CC QWYZFXLSWMXLDM-UHFFFAOYSA-M 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
- OASCYHRIQHKJKX-UHFFFAOYSA-N 1-(1,3,3-Trimethyl-2,3-dihydro-1H-indol-2-yliden)acetone Chemical compound C1=CC=C2N(C)C(=CC(C)=O)C(C)(C)C2=C1 OASCYHRIQHKJKX-UHFFFAOYSA-N 0.000 description 1
- WOWQRINVJIZXNR-UHFFFAOYSA-N 2-(2-methoxyprop-1-enyl)-1,3-benzothiazole Chemical compound C1=CC=C2SC(C=C(C)OC)=NC2=C1 WOWQRINVJIZXNR-UHFFFAOYSA-N 0.000 description 1
- XQWPDHWIZIUXDD-UHFFFAOYSA-N 4-chloro-2-methoxy-1,3-benzothiazole Chemical compound C1=CC=C2SC(OC)=NC2=C1Cl XQWPDHWIZIUXDD-UHFFFAOYSA-N 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- UNMYWSMUMWPJLR-UHFFFAOYSA-L Calcium iodide Chemical compound [Ca+2].[I-].[I-] UNMYWSMUMWPJLR-UHFFFAOYSA-L 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 241001165575 Hylotelephium telephium subsp. maximum Species 0.000 description 1
- 244000172533 Viola sororia Species 0.000 description 1
- BOXNENYOGRMVAM-UHFFFAOYSA-L [Na+].[Na+].[O-]P([O-])(Cl)=O Chemical compound [Na+].[Na+].[O-]P([O-])(Cl)=O BOXNENYOGRMVAM-UHFFFAOYSA-L 0.000 description 1
- CRNDXTILTKYGQA-UHFFFAOYSA-N [Na].OCl(=O)(=O)=O Chemical compound [Na].OCl(=O)(=O)=O CRNDXTILTKYGQA-UHFFFAOYSA-N 0.000 description 1
- 206010000269 abscess Diseases 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000002075 anti-alcohol Effects 0.000 description 1
- 229940046413 calcium iodide Drugs 0.000 description 1
- 229910001640 calcium iodide Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229930002875 chlorophyll Natural products 0.000 description 1
- 235000019804 chlorophyll Nutrition 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- ICIWUVCWSCSTAQ-UHFFFAOYSA-M iodate Chemical compound [O-]I(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-M 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- ZDGGJQMSELMHLK-UHFFFAOYSA-N m-Trifluoromethylhippuric acid Chemical compound OC(=O)CNC(=O)C1=CC=CC(C(F)(F)F)=C1 ZDGGJQMSELMHLK-UHFFFAOYSA-N 0.000 description 1
- 230000001537 neural effect Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU645571A3 (ru) | Способ получени производных хиназолона или их солей | |
| DE2718741A1 (de) | Cephalosporinverbindungen und verfahren zu deren herstellung | |
| EP2044062A1 (en) | Indole compounds | |
| JPH04234844A (ja) | 新規化合物の3−アミノ−2−オキソアゼチジン誘導体及びそれらの製造法 | |
| BR112012004161B1 (pt) | método para sintetizar uma piperazina neuroestimulativa | |
| SU93341A1 (https=) | ||
| SU1282814A3 (ru) | Способ получени производных малеинимида и сукцинимида | |
| CN102395582A (zh) | 伊潘立酮的一种制备方法及结晶方法 | |
| BR112012006233B1 (pt) | Composto de fórmula i, composição farmacêutica e usos de um composto | |
| SU576947A3 (ru) | Способ получени производных цефалоспорина или их солей | |
| SU107123A1 (ru) | Способ получени тетра- и гексаметингемициановых красителей | |
| CN115477645A (zh) | 马来酸阿伐曲泊帕系列杂质及其制备方法和应用 | |
| CN115974851A (zh) | 2-氧代-3-氮杂双环[3.1.0]己烷衍生物 | |
| SU109457A1 (ru) | Способ получени симметричных и несимметричных трикарбоцианиновых красителей | |
| SU1076433A1 (ru) | Способ получени имидамероцианиноцианиновых красителей | |
| SU113692A1 (ru) | Способ получени родацианиновых красителей | |
| SU106918A1 (ru) | Способ получени гексаметингемицианиновых красителей | |
| SU244887A1 (https=) | ||
| SU493757A1 (ru) | Способ получени дикарбоцианиновых красителей | |
| SU115961A2 (ru) | Способ получени родацианиновых красителей | |
| SU170595A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ ЧЕТЫРЕХЪЯДЕРНЫХ ПОЛИМЕТИНОВЫХКРАСИТЕЛЕЙ12Предложен способ получени четырехъ- дерных полиметиновых красителей общего строени I. Эти красители получают нагреванием оксаниноцианинов П с алкилирующими веществами, в частности, с диалкилсульфата- ми, и конденсацией образующихс четвертичных солей III с циклическими кетометиленовы- ми соединени ми IV или их этилидензамещен- ными V.п,с=с—в о=с—IYСНз-С=С- - В )10СН=1'/(CH-ClrC--,с--//R"15где Zостатки азотистых гетероциклических оснований, например бензтиазола, бензселеназола, тиазола, пиридина и др.;V—О, S, Se или NR; R—алкил, R'nR"—алкил или арпл;В—остатки циклических кетометилено- вых соединений, например 3-алкил- роданина, Ьфенил-З-метилпиразоло- на, тиогидантоипа и др.; А—Н, СНз НЛП ОСоН^; п—О или 1;X — кислотный остаток.2025о=с--S—г^Н=1N I"^^lЛ' 'IR"^11~Т^^ I ^^" А о"^SR | |
| SU117172A1 (ru) | Способ получени симметричных карбоцианиновых красителей | |
| SU94257A1 (ru) | Способ получени тиадикарбоцаниновых красителей с аминогруппой в бета-положении полиметиновой цепи | |
| SU162902A1 (https=) | ||
| SU93725A1 (ru) | Способ получени полиметиновых красителей (7-алкоксиродакарбоцианинов) |