SU561504A3 - Способ получени 2,2",3,3"тетракарбоксидиангидрида дифенилового эфира - Google Patents
Способ получени 2,2",3,3"тетракарбоксидиангидрида дифенилового эфираInfo
- Publication number
- SU561504A3 SU561504A3 SU2034558A SU2034558A SU561504A3 SU 561504 A3 SU561504 A3 SU 561504A3 SU 2034558 A SU2034558 A SU 2034558A SU 2034558 A SU2034558 A SU 2034558A SU 561504 A3 SU561504 A3 SU 561504A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- diphenyl ether
- tetracarboxydiphenyl
- obtaining
- parts
- metal nitrite
- Prior art date
Links
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 title claims 4
- 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 claims description 2
- 150000008064 anhydrides Chemical class 0.000 claims description 2
- 229910052792 caesium Inorganic materials 0.000 claims description 2
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 2
- 229910052701 rubidium Inorganic materials 0.000 claims description 2
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 2
- -1 alkaline earth metal nitrite Chemical class 0.000 claims 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 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 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- AZFNGPAYDKGCRB-XCPIVNJJSA-M [(1s,2s)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1-methyl-4-propan-2-ylbenzene Chemical compound [Ru+]Cl.CC(C)C1=CC=C(C)C=C1.C1=CC(C)=CC=C1S(=O)(=O)[N-][C@@H](C=1C=CC=CC=1)[C@@H](N)C1=CC=CC=C1 AZFNGPAYDKGCRB-XCPIVNJJSA-M 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 150000001243 acetic acids Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 235000010289 potassium nitrite Nutrition 0.000 description 1
- 239000004304 potassium nitrite Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/54—Preparation of carboxylic acid anhydrides
- C07C51/567—Preparation of carboxylic acid anhydrides by reactions not involving carboxylic acid anhydride groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Furan Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37277173A | 1973-06-22 | 1973-06-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU561504A3 true SU561504A3 (ru) | 1977-06-05 |
Family
ID=23469576
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU2034558A SU561504A3 (ru) | 1973-06-22 | 1974-06-14 | Способ получени 2,2",3,3"тетракарбоксидиангидрида дифенилового эфира |
Country Status (10)
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5185451A (en) * | 1989-05-15 | 1993-02-09 | Occidental Chemical Corporation | Bis-imides of dioxydiphthalic acid |
| US5166404A (en) * | 1989-05-15 | 1992-11-24 | Occidental Chemical Corporation | Dioxydiphthalic acid esters |
| CN108350148A (zh) * | 2015-03-19 | 2018-07-31 | 衡所华威电子有限公司 | 使用酸酐硬化剂的环氧模塑化合物、其制备方法和用途 |
-
1974
- 1974-04-05 DE DE19742416594 patent/DE2416594C2/de not_active Expired
- 1974-05-02 GB GB1931574A patent/GB1467275A/en not_active Expired
- 1974-06-14 SU SU2034558A patent/SU561504A3/ru active
- 1974-06-19 SE SE7408147A patent/SE412226B/xx not_active IP Right Cessation
- 1974-06-20 IT IT2420374A patent/IT1015232B/it active
- 1974-06-20 DK DK332774A patent/DK143400C/da not_active IP Right Cessation
- 1974-06-20 DD DD17933074A patent/DD112430A5/xx unknown
- 1974-06-20 JP JP6974974A patent/JPS5850992B2/ja not_active Expired
- 1974-06-21 FR FR7421578A patent/FR2299331A1/fr active Granted
- 1974-06-21 BR BR507074A patent/BR7405070D0/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB1467275A (en) | 1977-03-16 |
| SE412226B (sv) | 1980-02-25 |
| DK143400C (da) | 1981-12-21 |
| AU6775674A (en) | 1975-10-16 |
| DE2416594A1 (de) | 1975-01-16 |
| DK332774A (enrdf_load_stackoverflow) | 1975-03-17 |
| FR2299331B1 (enrdf_load_stackoverflow) | 1979-02-23 |
| JPS5032143A (enrdf_load_stackoverflow) | 1975-03-28 |
| BR7405070D0 (pt) | 1975-01-21 |
| DK143400B (da) | 1981-08-17 |
| DE2416594C2 (de) | 1983-12-08 |
| JPS5850992B2 (ja) | 1983-11-14 |
| SE7408147L (enrdf_load_stackoverflow) | 1974-12-23 |
| DD112430A5 (enrdf_load_stackoverflow) | 1975-04-12 |
| IT1015232B (it) | 1977-05-10 |
| FR2299331A1 (fr) | 1976-08-27 |
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