JP2010540414A5 - - Google Patents
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- Publication number
- JP2010540414A5 JP2010540414A5 JP2010524457A JP2010524457A JP2010540414A5 JP 2010540414 A5 JP2010540414 A5 JP 2010540414A5 JP 2010524457 A JP2010524457 A JP 2010524457A JP 2010524457 A JP2010524457 A JP 2010524457A JP 2010540414 A5 JP2010540414 A5 JP 2010540414A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- alkyl
- substituted
- hydroxy
- 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
- 150000001875 compounds Chemical class 0.000 claims 15
- 238000000034 method Methods 0.000 claims 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 229910021536 Zeolite Inorganic materials 0.000 claims 4
- 239000003054 catalyst Substances 0.000 claims 4
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
- 239000002904 solvent Substances 0.000 claims 4
- 239000010457 zeolite Substances 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 3
- 125000001072 heteroaryl group Chemical group 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- -1 iodine Chemical compound 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 3
- 125000000962 organic group Chemical group 0.000 claims 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 125000001207 fluorophenyl group Chemical group 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000006501 nitrophenyl group Chemical group 0.000 claims 2
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 229960002317 succinimide Drugs 0.000 claims 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 2
- 229920002554 vinyl polymer Polymers 0.000 claims 2
- RSEBUVRVKCANEP-UHFFFAOYSA-N 2-pyrroline Chemical compound C1CC=CN1 RSEBUVRVKCANEP-UHFFFAOYSA-N 0.000 claims 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 239000012467 final product Substances 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- ZVJHJDDKYZXRJI-UHFFFAOYSA-N pyrroline Natural products C1CC=NC1 ZVJHJDDKYZXRJI-UHFFFAOYSA-N 0.000 claims 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims 1
- PNGLEYLFMHGIQO-UHFFFAOYSA-M sodium;3-(n-ethyl-3-methoxyanilino)-2-hydroxypropane-1-sulfonate;dihydrate Chemical compound O.O.[Na+].[O-]S(=O)(=O)CC(O)CN(CC)C1=CC=CC(OC)=C1 PNGLEYLFMHGIQO-UHFFFAOYSA-M 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07116371.1 | 2007-09-13 | ||
| EP07116371A EP2036898A2 (de) | 2007-09-13 | 2007-09-13 | Verfahren zur Herstellung von 1,3-Dioxolan-2Onen sowie von Carbonsäureestern durch Transacylierung unter Basischen Reaktionsbedingungen |
| PCT/EP2008/061618 WO2009037111A2 (de) | 2007-09-13 | 2008-09-03 | Verfahren zur herstellung von 1,3-dioxolan-2-onen sowie von carbonsäureestern durch transacylierung unter basischen reaktionsbedingungen |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013186485A Division JP2014058515A (ja) | 2007-09-13 | 2013-09-09 | 塩基性反応条件下におけるアシル転位によって１，３−ジオキソラン−２−オン及びカルボン酸エステルを調製する方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010540414A JP2010540414A (ja) | 2010-12-24 |
| JP2010540414A5 true JP2010540414A5 (enExample) | 2011-05-26 |
| JP5567480B2 JP5567480B2 (ja) | 2014-08-06 |
Family
ID=39148452
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010524457A Active JP5567480B2 (ja) | 2007-09-13 | 2008-09-03 | 塩基性反応条件下におけるアシル転位によって１，３−ジオキソラン−２−オン及びカルボン酸エステルを調製する方法 |
| JP2013186485A Pending JP2014058515A (ja) | 2007-09-13 | 2013-09-09 | 塩基性反応条件下におけるアシル転位によって１，３−ジオキソラン−２−オン及びカルボン酸エステルを調製する方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013186485A Pending JP2014058515A (ja) | 2007-09-13 | 2013-09-09 | 塩基性反応条件下におけるアシル転位によって１，３−ジオキソラン−２−オン及びカルボン酸エステルを調製する方法 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8263788B2 (enExample) |
| EP (2) | EP2036898A2 (enExample) |
| JP (2) | JP5567480B2 (enExample) |
| CA (1) | CA2699909A1 (enExample) |
| WO (1) | WO2009037111A2 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9256125B2 (en) * | 2013-03-30 | 2016-02-09 | Rohm And Haas Electronic Materials, Llc | Acid generators and photoresists comprising same |
| TWI884957B (zh) * | 2019-05-24 | 2025-06-01 | 德商巴地斯顏料化工廠 | 用於生產2,2,6,6-四甲基-4-哌啶酮的非勻相催化方法 |
| IT202300015726A1 (it) | 2023-10-05 | 2025-04-05 | Isuschem S R L | Catalizzatori a base di fe(ii) e fe(iii) per la reazioni di chetalizzazione di a-idrossiacidi |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1301254A (enExample) * | 1971-07-08 | 1972-12-29 | ||
| US4384879A (en) * | 1980-07-15 | 1983-05-24 | Ciba-Geigy Corporation | 4-(1H-Azolylmethyl)-1,3-dioxolan-5-one derivatives, production thereof and use thereof as growth regulators and/or microbicides |
| DE10064816A1 (de) * | 2000-12-22 | 2002-06-27 | Boehringer Ingelheim Pharma | Verfahren zur Herstellung eines Anticholinergikums |
| DE102005035112A1 (de) * | 2005-07-27 | 2007-02-15 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neues Verfahren zur Herstellung von Tiotropiumsalzen unter Anwendung von in organischen Lösungsmitteln löslichen N-Methylscopiniumsalzen |
-
2007
- 2007-09-13 EP EP07116371A patent/EP2036898A2/de not_active Ceased
-
2008
- 2008-09-03 WO PCT/EP2008/061618 patent/WO2009037111A2/de not_active Ceased
- 2008-09-03 US US12/677,920 patent/US8263788B2/en active Active
- 2008-09-03 JP JP2010524457A patent/JP5567480B2/ja active Active
- 2008-09-03 CA CA2699909A patent/CA2699909A1/en not_active Abandoned
- 2008-09-03 EP EP08803589.4A patent/EP2190831B1/de active Active
-
2013
- 2013-09-09 JP JP2013186485A patent/JP2014058515A/ja active Pending
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