JP2004519513A5 - - Google Patents
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- Publication number
- JP2004519513A5 JP2004519513A5 JP2002577786A JP2002577786A JP2004519513A5 JP 2004519513 A5 JP2004519513 A5 JP 2004519513A5 JP 2002577786 A JP2002577786 A JP 2002577786A JP 2002577786 A JP2002577786 A JP 2002577786A JP 2004519513 A5 JP2004519513 A5 JP 2004519513A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- zsm
- compound
- ethyl ketone
- molecular formula
- 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.)
- Granted
Links
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 27
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 18
- GFYHSKONPJXCDE-UHFFFAOYSA-N 2,3,5-trimethylpyridine Chemical compound CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 claims description 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 10
- UTBIMNXEDGNJFE-UHFFFAOYSA-N 2,3,6-trimethylpyridine Chemical compound CC1=CC=C(C)C(C)=N1 UTBIMNXEDGNJFE-UHFFFAOYSA-N 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 229910021529 ammonia Inorganic materials 0.000 claims description 5
- 239000002994 raw material Substances 0.000 claims description 3
- 238000010189 synthetic method Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- 229910021536 Zeolite Inorganic materials 0.000 claims 3
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000010457 zeolite Substances 0.000 claims 3
- ZAAVUWIYUMVQJG-UHFFFAOYSA-N 2,3,5,6-tetramethylpyridine Chemical compound CC1=CC(C)=C(C)N=C1C ZAAVUWIYUMVQJG-UHFFFAOYSA-N 0.000 claims 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
- 238000001308 synthesis method Methods 0.000 claims 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- 239000010941 cobalt Substances 0.000 claims 1
- 229910017052 cobalt Inorganic materials 0.000 claims 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims 1
- 229910052802 copper Inorganic materials 0.000 claims 1
- 239000010949 copper Substances 0.000 claims 1
- 239000007789 gas Substances 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- 229910052742 iron Inorganic materials 0.000 claims 1
- 229910052746 lanthanum Inorganic materials 0.000 claims 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims 1
- 239000011133 lead Substances 0.000 claims 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 230000002194 synthesizing effect Effects 0.000 claims 1
- BKCIQPUIDHPJSI-UHFFFAOYSA-N 2,3,4,5-tetramethylpyridine Chemical compound CC1=CN=C(C)C(C)=C1C BKCIQPUIDHPJSI-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- COHDGTRFTKHYSJ-UHFFFAOYSA-N 2-Ethyl-5-methylpyridine Chemical compound CCC1=CC=C(C)C=N1 COHDGTRFTKHYSJ-UHFFFAOYSA-N 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/IN2001/000063 WO2002079159A1 (en) | 2001-03-30 | 2001-03-30 | A process for the preparation of a collidine and 2,3,5,6-tetramethyl pyridine |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004519513A JP2004519513A (ja) | 2004-07-02 |
| JP2004519513A5 true JP2004519513A5 (enExample) | 2005-05-19 |
| JP4040471B2 JP4040471B2 (ja) | 2008-01-30 |
Family
ID=27799860
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002577786A Expired - Fee Related JP4040471B2 (ja) | 2001-03-30 | 2001-03-30 | ２，３，５−トリメチルピリジン、２，３，６−トリメチルピリジン及び２，３，５，６−テトラメチルピリジンの製造方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6495695B2 (enExample) |
| EP (1) | EP1347961B1 (enExample) |
| JP (1) | JP4040471B2 (enExample) |
| CN (1) | CN1224615C (enExample) |
| AT (1) | ATE382606T1 (enExample) |
| BR (1) | BR0114507A (enExample) |
| DE (1) | DE60132245D1 (enExample) |
| WO (1) | WO2002079159A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101623636B (zh) * | 2009-08-11 | 2011-11-16 | 沙隆达集团公司 | 一种吡啶和烷基吡啶合成催化剂及其制备方法 |
| TWI598335B (zh) | 2012-10-25 | 2017-09-11 | Ｗ Ｒ 康格雷氏公司 | 用於製造吡啶及其烷基衍生物之改良方法、觸媒 |
| RU2688224C1 (ru) * | 2017-12-25 | 2019-05-21 | Федеральное государственное бюджетное учреждение науки Институт нефтехимии и катализа Российской академии наук | Способ получения пиридинов |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2059781T3 (es) * | 1988-10-28 | 1994-11-16 | Nepera Inc | Sintesis con alto rendimiento de piridina y/o alquilpiridina(s) a traves de condensacion de mezclas ternarias de aldehidos y/o cetonas con amoniaco. |
| JP4313854B2 (ja) * | 1997-06-16 | 2009-08-12 | 広栄化学工業株式会社 | ２，３，５−コリジン及び２−エチル−５−メチルピリジンの製造方法 |
-
2001
- 2001-03-27 US US09/818,279 patent/US6495695B2/en not_active Expired - Fee Related
- 2001-03-30 BR BR0114507-0A patent/BR0114507A/pt active Search and Examination
- 2001-03-30 WO PCT/IN2001/000063 patent/WO2002079159A1/en not_active Ceased
- 2001-03-30 JP JP2002577786A patent/JP4040471B2/ja not_active Expired - Fee Related
- 2001-03-30 EP EP01934293A patent/EP1347961B1/en not_active Expired - Lifetime
- 2001-03-30 CN CNB018166369A patent/CN1224615C/zh not_active Expired - Fee Related
- 2001-03-30 DE DE60132245T patent/DE60132245D1/de not_active Expired - Lifetime
- 2001-03-30 AT AT01934293T patent/ATE382606T1/de not_active IP Right Cessation
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