ES265099A1 - Procedimiento de obtenciën de piridil alkil ketonas - Google Patents
Procedimiento de obtenciën de piridil alkil ketonasInfo
- Publication number
- ES265099A1 ES265099A1 ES0265099A ES265099A ES265099A1 ES 265099 A1 ES265099 A1 ES 265099A1 ES 0265099 A ES0265099 A ES 0265099A ES 265099 A ES265099 A ES 265099A ES 265099 A1 ES265099 A1 ES 265099A1
- Authority
- ES
- Spain
- Prior art keywords
- pyridyl
- methyl ketone
- ketone
- water
- alumina
- 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
- -1 pyridyl alkyl ketones Chemical class 0.000 title abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 3
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 3
- 229930195729 fatty acid Natural products 0.000 abstract 3
- 239000000194 fatty acid Substances 0.000 abstract 3
- 150000004665 fatty acids Chemical class 0.000 abstract 3
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 abstract 2
- DASXLYSUTRIHGW-UHFFFAOYSA-N 1-(3-ethylpyridin-4-yl)ethanone Chemical compound CCC1=CN=CC=C1C(C)=O DASXLYSUTRIHGW-UHFFFAOYSA-N 0.000 abstract 1
- RLWNMLQDGSJZEL-UHFFFAOYSA-N 1-(5-acetylpyridin-3-yl)ethanone Chemical compound CC(=O)C1=CN=CC(C(C)=O)=C1 RLWNMLQDGSJZEL-UHFFFAOYSA-N 0.000 abstract 1
- DIASEPULVQSMAS-UHFFFAOYSA-N 1-(5-methylpyridin-3-yl)ethanone Chemical compound CC(=O)C1=CN=CC(C)=C1 DIASEPULVQSMAS-UHFFFAOYSA-N 0.000 abstract 1
- JORUAYHMUWRFNM-UHFFFAOYSA-N 1-pyridin-3-ylbutan-1-one Chemical compound CCCC(=O)C1=CC=CN=C1 JORUAYHMUWRFNM-UHFFFAOYSA-N 0.000 abstract 1
- QDCGHMZYGQRKSZ-UHFFFAOYSA-N 1-pyridin-3-yloctadecan-1-one Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)C=1C=NC=CC1 QDCGHMZYGQRKSZ-UHFFFAOYSA-N 0.000 abstract 1
- WMQUKDQWMMOHSA-UHFFFAOYSA-N 1-pyridin-4-ylethanone Chemical compound CC(=O)C1=CC=NC=C1 WMQUKDQWMMOHSA-UHFFFAOYSA-N 0.000 abstract 1
- AJKVQEKCUACUMD-UHFFFAOYSA-N 2-Acetylpyridine Chemical compound CC(=O)C1=CC=CC=N1 AJKVQEKCUACUMD-UHFFFAOYSA-N 0.000 abstract 1
- FFNVQNRYTPFDDP-UHFFFAOYSA-N 2-cyanopyridine Chemical compound N#CC1=CC=CC=N1 FFNVQNRYTPFDDP-UHFFFAOYSA-N 0.000 abstract 1
- WEGYGNROSJDEIW-UHFFFAOYSA-N 3-Acetylpyridine Chemical compound CC(=O)C1=CC=CN=C1 WEGYGNROSJDEIW-UHFFFAOYSA-N 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 abstract 1
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 abstract 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 abstract 1
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 229910000423 chromium oxide Inorganic materials 0.000 abstract 1
- 239000000571 coke Substances 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 238000011065 in-situ storage Methods 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- OOAWCECZEHPMBX-UHFFFAOYSA-N oxygen(2-);uranium(4+) Chemical compound [O-2].[O-2].[U+4] OOAWCECZEHPMBX-UHFFFAOYSA-N 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 150000004671 saturated fatty acids Chemical class 0.000 abstract 1
- 238000005979 thermal decomposition reaction Methods 0.000 abstract 1
- FCTBKIHDJGHPPO-UHFFFAOYSA-N uranium dioxide Inorganic materials O=[U]=O FCTBKIHDJGHPPO-UHFFFAOYSA-N 0.000 abstract 1
- 229910001935 vanadium oxide Inorganic materials 0.000 abstract 1
- 239000011787 zinc oxide Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/46—Oxygen atoms
- C07D213/50—Ketonic radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1526460A | 1960-03-16 | 1960-03-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES265099A1 true ES265099A1 (es) | 1962-07-01 |
Family
ID=21770421
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0265099A Expired ES265099A1 (es) | 1960-03-16 | 1961-02-22 | Procedimiento de obtenciën de piridil alkil ketonas |
Country Status (6)
| Country | Link |
|---|---|
| CH (1) | CH401051A (it) |
| DE (1) | DE1225182B (it) |
| DK (1) | DK102859C (it) |
| ES (1) | ES265099A1 (it) |
| GB (1) | GB920303A (it) |
| IT (1) | IT1029501B (it) |
-
1961
- 1961-02-03 IT IT183361A patent/IT1029501B/it active
- 1961-02-08 DE DER29626A patent/DE1225182B/de active Pending
- 1961-02-22 ES ES0265099A patent/ES265099A1/es not_active Expired
- 1961-03-01 GB GB745461A patent/GB920303A/en not_active Expired
- 1961-03-10 CH CH292561A patent/CH401051A/fr unknown
- 1961-03-15 DK DK110061A patent/DK102859C/da active
Also Published As
| Publication number | Publication date |
|---|---|
| DK102859C (da) | 1965-10-18 |
| DE1225182B (de) | 1966-09-22 |
| IT1029501B (it) | 1979-03-20 |
| CH401051A (fr) | 1965-10-31 |
| GB920303A (en) | 1963-03-06 |
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