SU633466A3 - Способ получени хальконовых эфиров - Google Patents
Способ получени хальконовых эфировInfo
- Publication number
- SU633466A3 SU633466A3 SU752302053A SU2302053A SU633466A3 SU 633466 A3 SU633466 A3 SU 633466A3 SU 752302053 A SU752302053 A SU 752302053A SU 2302053 A SU2302053 A SU 2302053A SU 633466 A3 SU633466 A3 SU 633466A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- ether
- methyl
- obtaining
- chalcone
- esters
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 2
- 150000001788 chalcone derivatives Chemical class 0.000 title 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 claims 1
- 150000008041 alkali metal carbonates Chemical class 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 27
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 22
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 238000003756 stirring Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229910000027 potassium carbonate Inorganic materials 0.000 description 5
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- LOYZVRIHVZEDMW-UHFFFAOYSA-N 1-bromo-3-methylbut-2-ene Chemical compound CC(C)=CCBr LOYZVRIHVZEDMW-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- JKXQKGNGJVZKFA-UHFFFAOYSA-N 1-chloro-3-methylbut-2-ene Chemical compound CC(C)=CCCl JKXQKGNGJVZKFA-UHFFFAOYSA-N 0.000 description 1
- LKNPFZQVNZFLIC-UHFFFAOYSA-N 2',4'-dihydroxychalcone Natural products OC1=CC(O)=CC=C1C=CC(=O)C1=CC=CC=C1 LKNPFZQVNZFLIC-UHFFFAOYSA-N 0.000 description 1
- LKNPFZQVNZFLIC-VQHVLOKHSA-N 2,4-Dihydroxychalcone Chemical compound OC1=CC(O)=CC=C1\C=C\C(=O)C1=CC=CC=C1 LKNPFZQVNZFLIC-VQHVLOKHSA-N 0.000 description 1
- ZFJUZUQNZJXFNH-UHFFFAOYSA-N CC(=CCOC1=C(C=CC(=C1)OCC=C(C)C)C=CC(=O)C1=CC=CC=C1)C Chemical compound CC(=CCOC1=C(C=CC(=C1)OCC=C(C)C)C=CC(=O)C1=CC=CC=C1)C ZFJUZUQNZJXFNH-UHFFFAOYSA-N 0.000 description 1
- DQFBYFPFKXHELB-UHFFFAOYSA-N Chalcone Natural products C=1C=CC=CC=1C(=O)C=CC1=CC=CC=C1 DQFBYFPFKXHELB-UHFFFAOYSA-N 0.000 description 1
- 229920004449 Halon® Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000005513 chalcones Nutrition 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- DQFBYFPFKXHELB-VAWYXSNFSA-N trans-chalcone Chemical compound C=1C=CC=CC=1C(=O)\C=C\C1=CC=CC=C1 DQFBYFPFKXHELB-VAWYXSNFSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP49016524A JPS598250B2 (ja) | 1974-02-09 | 1974-02-09 | カルコンエ−テルの合成法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU633466A3 true SU633466A3 (ru) | 1978-11-15 |
Family
ID=11918649
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU752302053A SU633466A3 (ru) | 1974-02-09 | 1975-12-26 | Способ получени хальконовых эфиров |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JPS598250B2 (cg-RX-API-DMAC7.html) |
| SU (1) | SU633466A3 (cg-RX-API-DMAC7.html) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ192641A (en) * | 1979-01-26 | 1984-10-19 | Hoffmann La Roche | Substituted acetophenones and pharmaceutical compositions |
| CA1137082A (en) * | 1979-05-23 | 1982-12-07 | Isao Umeda | Substituted acetophenones and process therefor |
-
1974
- 1974-02-09 JP JP49016524A patent/JPS598250B2/ja not_active Expired
-
1975
- 1975-12-26 SU SU752302053A patent/SU633466A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| JPS50108245A (cg-RX-API-DMAC7.html) | 1975-08-26 |
| JPS598250B2 (ja) | 1984-02-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0173714B1 (en) | Preparation of optically active 1,3-dioxolane-4-methanol compounds | |
| EP0043479A1 (en) | Novel cyclopentenone derivatives and methods for the preparation of the novel compounds | |
| SU633466A3 (ru) | Способ получени хальконовых эфиров | |
| US3835179A (en) | Novel 15-substituted prostanoic acids and esters | |
| US3406202A (en) | Preparation of aniline thioethers | |
| US2638484A (en) | Preparation of an octenone | |
| SU574149A3 (ru) | Способ получени циклопентановых производных или их солей | |
| US2768967A (en) | Process for manufacture of 2, 5 diketo-8-nonen-3-ol | |
| US2156721A (en) | Process of treating halogenated ketones | |
| US2376286A (en) | Process of making long chain intermediates | |
| US2159191A (en) | Process for the manufacture of levo-ascorbic acid | |
| SU374281A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ а-АРИЛПЕРФТОРПРОПИОНОВЫХ | |
| US2336093A (en) | 1-o-hydroxyphenoxy-3-alkoxy-2-propanols and/or-2-propanones and their manufacture | |
| US2102965A (en) | Manufacture of unsaturated aldehydes | |
| US2957027A (en) | Preparation of pseudo isomethyl ionone | |
| SU536160A1 (ru) | Способ получени 1-арил-3,3-дифенилпропанонов-1 | |
| SU425904A1 (ru) | Способ получения метилового эфира 4-диметиламино-5-хлор-0-анисовой кислоты | |
| SU475781A3 (ru) | Способ получени производных тиоуреидобензола | |
| SU396321A1 (ru) | Способ получения ацетиленовых аминоспиртов | |
| SU731889A3 (ru) | Способ получени производных бензилфенилкетона | |
| SU385956A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ а-АЛКОКСИ-а-(ЦИКЛОГЕКСЕН-2-ИЛ)- УКСУСНОЙ КИСЛОТЫ | |
| SU530023A1 (ru) | Способ получени циангидринов карнибольных соединений | |
| SU586168A1 (ru) | Способ выделени -аминозамещенного изомера из смеси производных -и -амино- -алкилтиокарбоновых кислот | |
| SU550389A1 (ru) | Способ получени шестичленных гетероциклических альдегидов | |
| SU456521A1 (ru) | Способ получени 5-аминобензодиоксана-1,4 |