SU414256A1 - - Google Patents
Info
- Publication number
- SU414256A1 SU414256A1 SU1777923A SU1777923A SU414256A1 SU 414256 A1 SU414256 A1 SU 414256A1 SU 1777923 A SU1777923 A SU 1777923A SU 1777923 A SU1777923 A SU 1777923A SU 414256 A1 SU414256 A1 SU 414256A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- acid
- mixture
- ozone
- target product
- another
- Prior art date
Links
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000003949 imides Chemical class 0.000 description 2
- 238000005949 ozonolysis reaction Methods 0.000 description 2
- JPJALAQPGMAKDF-UHFFFAOYSA-N selenium dioxide Chemical compound O=[Se]=O JPJALAQPGMAKDF-UHFFFAOYSA-N 0.000 description 2
- 101150043532 CISH gene Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 102100033979 Protein strawberry notch homolog 1 Human genes 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 1
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU1777923A SU414256A1 (enrdf_load_stackoverflow) | 1972-04-24 | 1972-04-24 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU1777923A SU414256A1 (enrdf_load_stackoverflow) | 1972-04-24 | 1972-04-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
SU414256A1 true SU414256A1 (enrdf_load_stackoverflow) | 1974-02-05 |
Family
ID=20512185
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU1777923A SU414256A1 (enrdf_load_stackoverflow) | 1972-04-24 | 1972-04-24 |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU414256A1 (enrdf_load_stackoverflow) |
-
1972
- 1972-04-24 SU SU1777923A patent/SU414256A1/ru active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4231934A (en) | Process for the production of N-(hydroxyphenyl) maleimides | |
JP4977353B2 (ja) | シクロブタンテトラカルボキシレート化合物及びその製造方法 | |
SU414256A1 (enrdf_load_stackoverflow) | ||
JPH0696545B2 (ja) | 3,5,6−トリフルオロ−4−ヒドロキシフタル酸の製造法 | |
SU567717A1 (ru) | Способ получени дифеновой кислоты | |
SU374277A1 (ru) | Способ получения 1, 2, 3, 4-пентантетракарбоновой кислотб1 или ее производных | |
SU1761749A1 (ru) | Способ получени N-(п-карбоксифенилен)-имида малеопимаровой кислоты | |
SU322984A1 (ru) | Способ получени 1,10-декандикарбо-НОВОй КиСлОТы | |
SU364618A1 (ru) | Способ получения диангидридов 1,2-бис- | |
SU1286596A1 (ru) | Способ получени 1-фенил-3-окси-1,2,3,4-тетрагидробензо @ -хинолина | |
SU1493641A1 (ru) | Способ получени 3-этилфталидов | |
SU569567A1 (ru) | Способ получени трет.-бутиловых моноперэфиров дикарбоновых кислот | |
US4324906A (en) | Citric acid esters and process for producing citric acid | |
RU1824395C (ru) | Способ выделени и очистки N,N @ -диметилимида 2,2-бис-[4-(3,4-дикарбоксифенокси)-фенил]пропана | |
SU437751A1 (ru) | Способ получени п-карбоксифенилимида-1,4,5-нафталинтрикарбоновой кислоты | |
SU1143745A1 (ru) | Способ получени производных 3-(3-бензоксазолонил)пропановой кислоты | |
SU345157A1 (ru) | Способ получения ангидридов или имидов з-сульфонобицикло | |
RU1838291C (ru) | Способ получени фумаровой кислоты | |
SU477997A1 (ru) | Способ получени -алкеновых кислот или их эфиров | |
SU958409A1 (ru) | Способ получени 2е-додецен-1,12-дикарбоновой кислоты | |
SU1696423A1 (ru) | Способ получени м-бензоилоксибензальдегида | |
SU825521A1 (ru) | Способ получени 2-ацилиндолов | |
SU1648943A1 (ru) | Способ получени дифтормалеиновой кислоты | |
SU1065408A1 (ru) | Способ получени 2-алкил-4-кетодигидрохиназолинов | |
SU565913A1 (ru) | Способ получени хлорнитроимидазолов |