GB1371118A - Process for the preparation of ketazines - Google Patents
Process for the preparation of ketazinesInfo
- Publication number
- GB1371118A GB1371118A GB1134372A GB1134372A GB1371118A GB 1371118 A GB1371118 A GB 1371118A GB 1134372 A GB1134372 A GB 1134372A GB 1134372 A GB1134372 A GB 1134372A GB 1371118 A GB1371118 A GB 1371118A
- Authority
- GB
- United Kingdom
- Prior art keywords
- radicals
- pentanol
- methyl
- formula
- ketazines
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000002360 preparation method Methods 0.000 title abstract 2
- -1 cycloalkyl radicals Chemical class 0.000 abstract 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 150000003254 radicals Chemical group 0.000 abstract 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- 229910021529 ammonia Inorganic materials 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 230000003647 oxidation Effects 0.000 abstract 2
- 238000007254 oxidation reaction Methods 0.000 abstract 2
- 150000003333 secondary alcohols Chemical class 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- JMSUNAQVHOHLMX-UHFFFAOYSA-N 1-cyclohexylethanol Chemical compound CC(O)C1CCCCC1 JMSUNAQVHOHLMX-UHFFFAOYSA-N 0.000 abstract 1
- WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 abstract 1
- WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 abstract 1
- PFLUPZGCTVGDLV-UHFFFAOYSA-N acetone azine Chemical compound CC(C)=NN=C(C)C PFLUPZGCTVGDLV-UHFFFAOYSA-N 0.000 abstract 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 abstract 1
- 125000002015 acyclic group Chemical group 0.000 abstract 1
- 238000007792 addition Methods 0.000 abstract 1
- 230000001476 alcoholic effect Effects 0.000 abstract 1
- 125000002723 alicyclic group Chemical group 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- XPNGNIFUDRPBFJ-UHFFFAOYSA-N alpha-methylbenzylalcohol Natural products CC1=CC=CC=C1CO XPNGNIFUDRPBFJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- KTHXBEHDVMTNOH-UHFFFAOYSA-N cyclobutanol Chemical compound OC1CCC1 KTHXBEHDVMTNOH-UHFFFAOYSA-N 0.000 abstract 1
- SFVWPXMPRCIVOK-UHFFFAOYSA-N cyclododecanol Chemical compound OC1CCCCCCCCCCC1 SFVWPXMPRCIVOK-UHFFFAOYSA-N 0.000 abstract 1
- QCRFMSUKWRQZEM-UHFFFAOYSA-N cycloheptanol Chemical compound OC1CCCCCC1 QCRFMSUKWRQZEM-UHFFFAOYSA-N 0.000 abstract 1
- FHADSMKORVFYOS-UHFFFAOYSA-N cyclooctanol Chemical compound OC1CCCCCCC1 FHADSMKORVFYOS-UHFFFAOYSA-N 0.000 abstract 1
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 abstract 1
- QILSFLSDHQAZET-UHFFFAOYSA-N diphenylmethanol Chemical compound C=1C=CC=CC=1C(O)C1=CC=CC=C1 QILSFLSDHQAZET-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000001033 ether group Chemical group 0.000 abstract 1
- 239000008246 gaseous mixture Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000007791 liquid phase Substances 0.000 abstract 1
- 150000001455 metallic ions Chemical class 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- KVKGYNYSUPXPRQ-UHFFFAOYSA-N nitro(oxido)azanium Chemical compound [O-][NH2+][N+]([O-])=O KVKGYNYSUPXPRQ-UHFFFAOYSA-N 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 abstract 1
- AQIXEPGDORPWBJ-UHFFFAOYSA-N pentan-3-ol Chemical compound CCC(O)CC AQIXEPGDORPWBJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000002978 peroxides Chemical class 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 239000012429 reaction media Substances 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 230000000087 stabilizing effect Effects 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/72—Hydrazones
- C07C251/88—Hydrazones having also the other nitrogen atom doubly-bound to a carbon atom, e.g. azines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7108509A FR2129016A5 (enrdf_load_stackoverflow) | 1971-03-11 | 1971-03-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1371118A true GB1371118A (en) | 1974-10-23 |
Family
ID=9073372
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1134372A Expired GB1371118A (en) | 1971-03-11 | 1972-03-10 | Process for the preparation of ketazines |
Country Status (15)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5317384U (enrdf_load_stackoverflow) * | 1976-07-22 | 1978-02-14 | ||
| FR2571711A1 (fr) * | 1984-10-16 | 1986-04-18 | Atochem | Procede de fabrication d'hydrate d'hydrazine |
-
1971
- 1971-03-11 FR FR7108509A patent/FR2129016A5/fr not_active Expired
-
1972
- 1972-03-07 DE DE2210790A patent/DE2210790C3/de not_active Expired
- 1972-03-09 ES ES400598A patent/ES400598A1/es not_active Expired
- 1972-03-09 ZA ZA721617A patent/ZA721617B/xx unknown
- 1972-03-10 BE BE780470A patent/BE780470A/xx not_active IP Right Cessation
- 1972-03-10 CA CA136,852A patent/CA967980A/en not_active Expired
- 1972-03-10 BR BR1380/72A patent/BR7201380D0/pt unknown
- 1972-03-10 NL NL7203200A patent/NL7203200A/xx not_active Application Discontinuation
- 1972-03-10 IT IT67770/72A patent/IT953949B/it active
- 1972-03-10 AU AU39905/72A patent/AU463391B2/en not_active Expired
- 1972-03-10 GB GB1134372A patent/GB1371118A/en not_active Expired
- 1972-03-10 CH CH357572A patent/CH551382A/fr not_active IP Right Cessation
- 1972-03-10 SE SE7203094A patent/SE389335B/xx unknown
- 1972-03-11 JP JP47024439A patent/JPS5133086B1/ja active Pending
- 1972-03-13 AT AT208872A patent/AT312572B/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| ZA721617B (en) | 1973-04-25 |
| DE2210790B2 (de) | 1978-07-20 |
| FR2129016A5 (enrdf_load_stackoverflow) | 1972-10-27 |
| DE2210790A1 (enrdf_load_stackoverflow) | 1972-10-05 |
| BE780470A (fr) | 1972-07-03 |
| AU3990572A (en) | 1973-09-13 |
| NL7203200A (enrdf_load_stackoverflow) | 1972-09-13 |
| JPS5133086B1 (enrdf_load_stackoverflow) | 1976-09-17 |
| BR7201380D0 (pt) | 1974-01-02 |
| DE2210790C3 (de) | 1979-03-15 |
| AU463391B2 (en) | 1975-07-08 |
| AT312572B (de) | 1974-01-10 |
| ES400598A1 (es) | 1975-02-01 |
| CA967980A (en) | 1975-05-20 |
| CH551382A (fr) | 1974-07-15 |
| SE389335B (sv) | 1976-11-01 |
| IT953949B (it) | 1973-08-10 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PE20 | Patent expired after termination of 20 years |