SU564804A3 - Способ получени производных дибензо /а, /циклогептена или их солей - Google Patents
Способ получени производных дибензо /а, /циклогептена или их солейInfo
- Publication number
- SU564804A3 SU564804A3 SU7502140475A SU2140475A SU564804A3 SU 564804 A3 SU564804 A3 SU 564804A3 SU 7502140475 A SU7502140475 A SU 7502140475A SU 2140475 A SU2140475 A SU 2140475A SU 564804 A3 SU564804 A3 SU 564804A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- oxo
- acid
- dihydrodibenzo
- calculated
- cycloheptenyl
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title claims 7
- 238000000034 method Methods 0.000 title claims 3
- QPJORFLSOJAUNL-UHFFFAOYSA-N dibenzo[a,d][7]annulene Chemical class C1=CC2=CC=CC=C2CC2=CC=CC=C21 QPJORFLSOJAUNL-UHFFFAOYSA-N 0.000 title 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- 239000002244 precipitate Substances 0.000 claims 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 239000000654 additive Chemical class 0.000 claims 2
- 230000000996 additive effect Effects 0.000 claims 2
- 239000012670 alkaline solution Substances 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 235000011121 sodium hydroxide Nutrition 0.000 claims 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 1
- 238000013019 agitation Methods 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- ZXIJMRYMVAMXQP-UHFFFAOYSA-N cycloheptene Chemical compound C1CCC=CCC1 ZXIJMRYMVAMXQP-UHFFFAOYSA-N 0.000 claims 1
- 150000001933 cycloheptenes Chemical class 0.000 claims 1
- 125000001162 cycloheptenyl group Chemical group C1(=CCCCCC1)* 0.000 claims 1
- 238000001914 filtration Methods 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical group 0.000 claims 1
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- 239000011707 mineral Substances 0.000 claims 1
- 235000010755 mineral Nutrition 0.000 claims 1
- 239000000047 product Substances 0.000 claims 1
- 229940080818 propionamide Drugs 0.000 claims 1
- 238000003756 stirring Methods 0.000 claims 1
- 239000000725 suspension Substances 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D317/18—Radicals substituted by singly bound oxygen or sulfur atoms
- C07D317/22—Radicals substituted by singly bound oxygen or sulfur atoms etherified
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
- C07C51/60—Preparation of carboxylic acid halides by conversion of carboxylic acids or their anhydrides or esters, lactones, salts into halides with the same carboxylic acid part
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/76—Unsaturated compounds containing keto groups
- C07C59/86—Unsaturated compounds containing keto groups containing six-membered aromatic rings and other rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7307508A FR2219777A1 (en) | 1973-03-02 | 1973-03-02 | 5-oxo dibenzo(a,d)cycloheptene derivs - with analgesic, antipyretic and anti-inflamm- atory activity |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU564804A3 true SU564804A3 (ru) | 1977-07-05 |
Family
ID=9115696
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU7502140475A SU564804A3 (ru) | 1973-03-02 | 1975-06-05 | Способ получени производных дибензо /а, /циклогептена или их солей |
Country Status (12)
| Country | Link |
|---|---|
| AR (1) | AR202847A1 (cs) |
| BE (1) | BE811794A (cs) |
| CH (1) | CH589033A5 (cs) |
| CS (1) | CS188196B2 (cs) |
| ES (1) | ES425405A1 (cs) |
| FR (1) | FR2219777A1 (cs) |
| HU (1) | HU168680B (cs) |
| NO (1) | NO783589L (cs) |
| PL (1) | PL97904B1 (cs) |
| SE (1) | SE413138B (cs) |
| SU (1) | SU564804A3 (cs) |
| ZA (1) | ZA741327B (cs) |
-
1973
- 1973-03-02 FR FR7307508A patent/FR2219777A1/fr active Granted
-
1974
- 1974-02-28 ZA ZA00741327A patent/ZA741327B/xx unknown
- 1974-02-28 CS CS763032A patent/CS188196B2/cs unknown
- 1974-03-01 BE BE141578A patent/BE811794A/xx unknown
- 1974-03-01 CH CH53277A patent/CH589033A5/xx not_active IP Right Cessation
- 1974-03-01 HU HURO827A patent/HU168680B/hu unknown
- 1974-03-02 PL PL1974188427A patent/PL97904B1/pl unknown
- 1974-04-17 ES ES425405A patent/ES425405A1/es not_active Expired
- 1974-10-15 AR AR256101A patent/AR202847A1/es active
-
1975
- 1975-06-05 SU SU7502140475A patent/SU564804A3/ru active
-
1976
- 1976-10-13 SE SE7611369A patent/SE413138B/xx unknown
-
1978
- 1978-10-24 NO NO78783589A patent/NO783589L/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AR202847A1 (es) | 1975-07-24 |
| ZA741327B (en) | 1975-02-26 |
| PL97904B1 (pl) | 1978-03-30 |
| FR2219777B1 (cs) | 1976-07-16 |
| ES425405A1 (es) | 1976-05-16 |
| BE811794A (fr) | 1974-09-02 |
| SE413138B (sv) | 1980-04-21 |
| NO783589L (no) | 1974-09-03 |
| CH589033A5 (cs) | 1977-06-30 |
| SE7611369L (sv) | 1976-10-13 |
| CS188196B2 (en) | 1979-02-28 |
| FR2219777A1 (en) | 1974-09-27 |
| HU168680B (cs) | 1976-06-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU508205A3 (ru) | Способ получени производных изофлавона | |
| SU439983A1 (ru) | Способ получени производных этиленбензоила | |
| US4144397A (en) | Preparation of 2-aryl-propionic acids by direct coupling utilizing a mixed magnesium halide complex | |
| US4528367A (en) | Method and intermediates for preparing high purity 3,3'-azo-bis-(6-hydroxy benzoic acid) | |
| KR100429082B1 (ko) | 1,2-벤즈이소티아졸린-3-온의제조방법 | |
| SU564804A3 (ru) | Способ получени производных дибензо /а, /циклогептена или их солей | |
| EP0135304B1 (en) | Preparation of substituted benzamides | |
| US5047553A (en) | Tetrafluoro-N-phenylphthalimide | |
| US5233082A (en) | Method of making 3-hydroxy-2,4,5-trifluorobenzoic acid | |
| HU182436B (en) | Process for producing 2,3,4,5-tetrahydro-1-benzoxepine-3,5-dion derivatives | |
| US4709075A (en) | Preparation of alkyl N-maleylphenylalanate | |
| US3412146A (en) | Process for preparation of diphenyl alkanoic acids | |
| US3818023A (en) | 2-phenyl benzothiazolyl acetic acid derivatives | |
| SU1304747A3 (ru) | Способ получени основных простых эфиров оксимов или их солей | |
| US4107179A (en) | Method for preparing ticrynafen | |
| SU507567A1 (ru) | Способ получени замещенных дитиокарбаматов | |
| SU1313856A1 (ru) | Способ получени производных цис- или транс-диаминодибензоилдибензо-18-краун-6 | |
| US5099043A (en) | 3-methylsulfonylmethyl-4-sulfomethyl-pyrrolidinium-betaines and process for their preparation | |
| US4316037A (en) | N-Benzyl and N-substituted benzyl tetrazole-5-carboxylic acids and the preparation thereof | |
| JP3563424B2 (ja) | 4h−ピラン−4−オンの製造方法 | |
| SU482039A3 (ru) | Способ получени бифенилилбутеновых кислот или их производных | |
| SU1426970A1 (ru) | Амиды о- пропенилбензойных кислот в качестве промежуточных продуктов в синтезе 3- этилфталимидинов | |
| BE858864A (fr) | Nouveaux esters d'acides phenyl- et pyridine-3-carboxylique et procede permettant leur preparation | |
| US4180510A (en) | Method for preparing thienylacetic acids | |
| SU960176A1 (ru) | Способ получени 2-ациламино-1,3,4-тиадиазолов |