SU571473A1 - Method of preparing lythium acrylate - Google Patents
Method of preparing lythium acrylateInfo
- Publication number
- SU571473A1 SU571473A1 SU7502127595A SU2127595A SU571473A1 SU 571473 A1 SU571473 A1 SU 571473A1 SU 7502127595 A SU7502127595 A SU 7502127595A SU 2127595 A SU2127595 A SU 2127595A SU 571473 A1 SU571473 A1 SU 571473A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- acrylic acid
- acrylate
- stirring
- hour
- product
- Prior art date
Links
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 title claims description 4
- 238000000034 method Methods 0.000 title description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 8
- 239000000047 product Substances 0.000 claims description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 claims description 5
- 229910052808 lithium carbonate Inorganic materials 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- XSAOIFHNXYIRGG-UHFFFAOYSA-M lithium;prop-2-enoate Chemical compound [Li+].[O-]C(=O)C=C XSAOIFHNXYIRGG-UHFFFAOYSA-M 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- 238000003756 stirring Methods 0.000 claims 3
- 229910002092 carbon dioxide Inorganic materials 0.000 claims 2
- 239000001569 carbon dioxide Substances 0.000 claims 2
- 239000002274 desiccant Substances 0.000 claims 2
- 238000001816 cooling Methods 0.000 claims 1
- 239000000706 filtrate Substances 0.000 claims 1
- 238000005086 pumping Methods 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N anhydrous n-heptane Natural products CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- QAZAAZKNSOCPBF-UHFFFAOYSA-N [Li].C(C=C)(=O)O Chemical compound [Li].C(C=C)(=O)O QAZAAZKNSOCPBF-UHFFFAOYSA-N 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000000155 isotopic effect Effects 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- -1 methyl alcohols Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
II
Изобретение относитс к способам получени металлоорганических соединений, а (менно литиевой соли акриловой кислоты.This invention relates to methods for producing organometallic compounds, a (lithium acrylic acid, lithium salt).
Известен способ получени щелочных солей акриловой кислоты взаимодействием предварительно нагретого до 30-50 С метилового или этилового эфира акриловой кислоты с 10-15%-HbtM водным раствором едкого натра, едкого кали или едкого пити , предварительно нагретым гю ЗО-90 С. Реакци : протекает при 60-15О С в течение 1-10 мин. Затем продукты реакции омыл ют добавлением эфиров1и ра9твора щелочи лри давлении 0,5-3,5 кг/см и температуре 9О-1О5 С l. Такой способ обеспечивает степень взаимодействи 99,5%.The known method of producing alkali salts of acrylic acid is the interaction of methyl or ethyl acrylic acid preheated to 30-50 ° C with 10-15% -HbtM aqueous sodium hydroxide, potassium hydroxide or caustic, preheated gy ZO-90 C. React: proceeds at 60-15 ° C for 1-10 minutes Then the reaction products are saponified by adding an alkali ester and an alkali solution at a pressure of 0.5-3.5 kg / cm and a temperature of 9O-1O5 C l. This method provides a 99.5% degree of interaction.
Недостатками этого способа вл ютс проведение реакции при повышенной температуре; ;невоаможность, получени акрилата. в чистом виде из-за присутстви полимерных продуктов, гидрохинона и исходных компонентов; двухступенчатый процесс получени .The disadvantages of this method are carrying out the reaction at elevated temperature; nevomazhnost, receiving acrylate. in its pure form due to the presence of polymer products, hydroquinone and the starting components; two-step production process.
С цепью повышени выходаи степени-чистоты целевого продукта по предлагаемомуWith a chain of increasing the yield of the degree of purity of the target product on the proposed
способу карбонат лити подвергают взаимо действию с акриловой кислотой при мол рном соотношении. 1:1 - 2 соответственно и температуре О-25 С в среде низшего ап канопа ,The lithium carbonate method is reacted with acrylic acid at a molar ratio. 1: 1 - 2, respectively, and the temperature O-25 C in the environment of the lowest up canopa,
Применение избытка акриловой кислоты позвол ет количественно весь карбонат лити перевести в акрилат лити . Последнее особенно важно при получении акрилата .0 лити изотопного состава. Дл удалени воды и избытка акриловой кислоты в реакционную смесь добавл ют, например, К1етчловый спирт и раствор пропускают через .колонку с окисью алюмини . Обработка с The use of an excess of acrylic acid allows quantitative conversion of all lithium carbonate to lithium acrylate. The latter is especially important when obtaining acrylate .0 lithium isotopic composition. To remove water and excess acrylic acid, for example, K1chl alcohol is added to the reaction mixture and the solution is passed through an alumina column. Processing with
и .окисью алюмини может быть заменена от мывкой сьфого продукта ацетоном или нормальными углеводородами.and alumina can be replaced by washing the finished product with acetone or normal hydrocarbons.
Акрилат лити очень хорошо раствориетс в акриловой кислоте, воде, несколько хуже в этиловом и метиловом спиртах, практически не раствор етс ; в эфире, ацетоне , бензоле, 1стироле,, нормальных гексане и гептане.Lithium acrylate is very well soluble in acrylic acid, water, slightly worse in ethyl and methyl alcohols, practically insoluble; in ether, acetone, benzene, 1-styrene,, normal hexane and heptane.
П р и м е р 1. К смеси, состо щей изPRI me R 1. To a mixture consisting of
Claims (2)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU7502127595A SU571473A1 (en) | 1975-04-23 | 1975-04-23 | Method of preparing lythium acrylate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU7502127595A SU571473A1 (en) | 1975-04-23 | 1975-04-23 | Method of preparing lythium acrylate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU571473A1 true SU571473A1 (en) | 1977-09-05 |
Family
ID=20617341
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU7502127595A SU571473A1 (en) | 1975-04-23 | 1975-04-23 | Method of preparing lythium acrylate |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU571473A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4404398A (en) * | 1978-01-12 | 1983-09-13 | Ppg Industries, Inc. | Preparation of unsaturated fluorocarbon acids |
-
1975
- 1975-04-23 SU SU7502127595A patent/SU571473A1/en active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4404398A (en) * | 1978-01-12 | 1983-09-13 | Ppg Industries, Inc. | Preparation of unsaturated fluorocarbon acids |
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