GB1097673A - Chlorination of alkyl and aralkyl pyridines - Google Patents
Chlorination of alkyl and aralkyl pyridinesInfo
- Publication number
- GB1097673A GB1097673A GB31851/64A GB3185164A GB1097673A GB 1097673 A GB1097673 A GB 1097673A GB 31851/64 A GB31851/64 A GB 31851/64A GB 3185164 A GB3185164 A GB 3185164A GB 1097673 A GB1097673 A GB 1097673A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aralkyl
- alkyl
- picoline
- pyridines
- chlorination
- 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
- 125000000217 alkyl group Chemical group 0.000 title abstract 4
- -1 aralkyl pyridines Chemical class 0.000 title abstract 4
- 238000005660 chlorination reaction Methods 0.000 title abstract 3
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 abstract 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 3
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 abstract 2
- ITQTTZVARXURQS-UHFFFAOYSA-N 3-methylpyridine Chemical compound CC1=CC=CN=C1 ITQTTZVARXURQS-UHFFFAOYSA-N 0.000 abstract 2
- FKNQCJSGGFJEIZ-UHFFFAOYSA-N 4-methylpyridine Chemical compound CC1=CC=NC=C1 FKNQCJSGGFJEIZ-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 239000003085 diluting agent Substances 0.000 abstract 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 2
- 230000035484 reaction time Effects 0.000 abstract 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 2
- NRGGMCIBEHEAIL-UHFFFAOYSA-N 2-ethylpyridine Chemical compound CCC1=CC=CC=N1 NRGGMCIBEHEAIL-UHFFFAOYSA-N 0.000 abstract 1
- XWKFPIODWVPXLX-UHFFFAOYSA-N 2-methyl-5-methylpyridine Natural products CC1=CC=C(C)N=C1 XWKFPIODWVPXLX-UHFFFAOYSA-N 0.000 abstract 1
- PFYPDUUXDADWKC-UHFFFAOYSA-N 2-propan-2-ylpyridine Chemical compound CC(C)C1=CC=CC=N1 PFYPDUUXDADWKC-UHFFFAOYSA-N 0.000 abstract 1
- DBOLXXRVIFGDTI-UHFFFAOYSA-N 4-benzylpyridine Chemical compound C=1C=NC=CC=1CC1=CC=CC=C1 DBOLXXRVIFGDTI-UHFFFAOYSA-N 0.000 abstract 1
- VJXRKZJMGVSXPX-UHFFFAOYSA-N 4-ethylpyridine Chemical compound CCC1=CC=NC=C1 VJXRKZJMGVSXPX-UHFFFAOYSA-N 0.000 abstract 1
- NTSLROIKFLNUIJ-UHFFFAOYSA-N 5-Ethyl-2-methylpyridine Chemical compound CCC1=CC=C(C)N=C1 NTSLROIKFLNUIJ-UHFFFAOYSA-N 0.000 abstract 1
- KNCHDRLWPAKSII-UHFFFAOYSA-N 5-ethyl-2-methylpyridine Natural products CCC1=CC=NC(C)=C1 KNCHDRLWPAKSII-UHFFFAOYSA-N 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 239000000571 coke Substances 0.000 abstract 1
- 239000003701 inert diluent Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 229910052573 porcelain Inorganic materials 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 abstract 1
- 229910010271 silicon carbide Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
-
- 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
- C07D213/26—Radicals substituted by halogen atoms or nitro radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL132136D NL132136C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1964-08-05 | ||
| GB31851/64A GB1097673A (en) | 1964-08-05 | 1964-08-05 | Chlorination of alkyl and aralkyl pyridines |
| US475558A US3412095A (en) | 1964-08-05 | 1965-07-28 | Chlorination of alkyl pyridines |
| FR26246A FR1445038A (fr) | 1964-08-05 | 1965-07-28 | Chloration des pyridines et des quinoléines alcoyles |
| NL6510041A NL6510041A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1964-08-05 | 1965-08-03 | |
| DE19651595948 DE1595948A1 (de) | 1964-08-05 | 1965-08-04 | Verfahren zur Herstellung chlorierter Alkyl-Pyridine und-Chinoline |
| BE667939D BE667939A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1964-08-05 | 1965-08-05 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB31851/64A GB1097673A (en) | 1964-08-05 | 1964-08-05 | Chlorination of alkyl and aralkyl pyridines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1097673A true GB1097673A (en) | 1968-01-03 |
Family
ID=10329348
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB31851/64A Expired GB1097673A (en) | 1964-08-05 | 1964-08-05 | Chlorination of alkyl and aralkyl pyridines |
Country Status (5)
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0042696A1 (en) * | 1980-06-19 | 1981-12-30 | Ishihara Sangyo Kaisha Ltd. | Process for producing trifluoromethylpyridines |
| US5484929A (en) * | 1993-09-21 | 1996-01-16 | Reilly Industries | Chlorination process |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4753673A (en) * | 1977-07-22 | 1988-06-28 | The Dow Chemical Company | Trifluoromethyl pyridinyloxyphenoxy and pyridinylthiophenoxy propanoic acids and propanols and derivatives thereof and methods of herbicidal use |
| DE2862492D1 (en) * | 1977-08-12 | 1988-09-01 | Ici Plc | Herbicidal halogenomethyl--pyridyloxy-phenoxy-alkanecarboxylic acids and derivatives, and processes of controlling unwanted plants therewith |
| JPH0224818B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1978-02-15 | 1990-05-30 | Imuperiaru Chem Ind Plc | |
| JPS5543017A (en) * | 1978-09-22 | 1980-03-26 | Ishihara Sangyo Kaisha Ltd | Preparation of 2-chloro-5-trichloromethylpyridine |
| NZ192948A (en) * | 1979-03-09 | 1982-02-23 | Ishihara Sangyo Kaisha | Preparation of beta-trifuloromethyl-pyridine derivatives directly from beta-picoline |
| HU188235B (en) * | 1982-12-11 | 1986-03-28 | Alkaloida Vegyeszeti Gyar,Hu | Process for producing fluoro-methyl-quinoline derivatives |
| US4483993A (en) * | 1983-04-08 | 1984-11-20 | Kalama Chemical, Inc. | Production of polychlorinated pyridine mixtures by liquid phase chlorination of beta-picoline or beta-picoline hydrochloride |
| US4713460A (en) * | 1986-07-22 | 1987-12-15 | The Dow Chemical Company | 2,3-bis-(poly)(chloromethyl)pyridines |
| DE3934957A1 (de) * | 1989-10-20 | 1991-04-25 | Bayer Ag | Verfahren zur herstellung von 3-trichlormethyl-pyridin |
| US5247093A (en) * | 1992-12-15 | 1993-09-21 | Reilly Industries, Inc. | Chlorination process |
| US5521316A (en) * | 1994-05-20 | 1996-05-28 | Cytec Technology Corp. | Chloroalkyl pyridinum hydrochloride compounds and processes for their preparation |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2585091A (en) * | 1947-11-14 | 1952-02-12 | Texas Co | Side chain halogenation of alkyl thiophenes |
| US2679453A (en) * | 1952-10-10 | 1954-05-25 | Charles H Brett | Method and composition for the control of undesired vegetation |
| NL302999A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1963-01-28 | |||
| US3251848A (en) * | 1963-11-12 | 1966-05-17 | Dow Chemical Co | Vapor phase production of 2-chloropyridine and 2, 6-dichloropyridine |
-
0
- NL NL132136D patent/NL132136C/xx active
-
1964
- 1964-08-05 GB GB31851/64A patent/GB1097673A/en not_active Expired
-
1965
- 1965-07-28 US US475558A patent/US3412095A/en not_active Expired - Lifetime
- 1965-08-03 NL NL6510041A patent/NL6510041A/xx unknown
- 1965-08-04 DE DE19651595948 patent/DE1595948A1/de active Pending
- 1965-08-05 BE BE667939D patent/BE667939A/xx unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0042696A1 (en) * | 1980-06-19 | 1981-12-30 | Ishihara Sangyo Kaisha Ltd. | Process for producing trifluoromethylpyridines |
| US4563529A (en) * | 1980-06-19 | 1986-01-07 | Ishihara Sangyo Kaisha Ltd. | Process for producing trifluoromethylpyridines |
| US5484929A (en) * | 1993-09-21 | 1996-01-16 | Reilly Industries | Chlorination process |
Also Published As
| Publication number | Publication date |
|---|---|
| US3412095A (en) | 1968-11-19 |
| NL132136C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| BE667939A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1966-02-07 |
| DE1595948A1 (de) | 1970-02-05 |
| NL6510041A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1966-02-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1097673A (en) | Chlorination of alkyl and aralkyl pyridines | |
| GB1395926A (en) | Process for the production of isoprene by the chlorination/ dehydrochlorination of 2-methylbutene-2 | |
| GB8724561D0 (en) | Production process | |
| GB1041906A (en) | Process for the production of chlorinated derivatives of pyridine | |
| DE3463044D1 (en) | Preparation of 2-chloro-5-methylpyridine | |
| GB1037122A (en) | Process for the production of 2-chloropyridine | |
| ES409241A1 (es) | Procedimiento para la obtencion de cloruro de vinilideno. | |
| GB1334922A (en) | Manufacture of halogenated pyridine derivatives | |
| GB1306517A (en) | Manufacture of halogenated pyridine derivatives | |
| GB902589A (en) | Production of hexafluoropropene and heptafluoropropane | |
| GB1019149A (en) | Improvements in or relating to the manufacture of 1,2,3,4-tetrachlorobutane | |
| Boudakian et al. | New synthesis routes to 2‐halopyridines. II. 2‐bromopyridine | |
| GB1152981A (en) | Improvements in or relating to the manufacture of Chlorinated Hydrocarbons | |
| GB1062768A (en) | Process for the production of perfluoro-propene | |
| GB1313791A (en) | Manufacture of 1,1-disubstituted-4,4-bipyridylium salts | |
| GB1208291A (en) | Catalytic process for the manufacture of pyridine and methylpyridines | |
| GB1019131A (en) | Improvements in or relating to the manufacture of 1,2,3,4-tetrachlorobutane | |
| GB869955A (en) | Improvements in and relating to the production of 2:2-dipyridyl | |
| HUT50321A (en) | Process for production of 2,3,5,6-tetrachlor-piridin and 2,3,6-trichlor-piridin | |
| HU9500261D0 (en) | Process for preparation of 1,1,1-trichloro-2,2,2-trifluoroethane | |
| GB1301724A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| GR3006678T3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| GB1037121A (en) | Process for the production of 2-bromopyridine | |
| GB1121295A (en) | The preparation of pyridine and alkyl-derivatives of pyridine | |
| GB1306562A (en) | Manufacture of halogenated pyridine derivatives |