JP2002525353A5 - - Google Patents
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- Publication number
- JP2002525353A5 JP2002525353A5 JP2000572188A JP2000572188A JP2002525353A5 JP 2002525353 A5 JP2002525353 A5 JP 2002525353A5 JP 2000572188 A JP2000572188 A JP 2000572188A JP 2000572188 A JP2000572188 A JP 2000572188A JP 2002525353 A5 JP2002525353 A5 JP 2002525353A5
- Authority
- JP
- Japan
- Prior art keywords
- ketal
- alkyl
- embedded image
- substituents
- 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
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- 125000001424 substituent group Chemical group 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- -1 phenyl-substituted methyl Chemical group 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 description 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 2
- 125000005262 alkoxyamine group Chemical group 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- 0 *C(C(C(*)=NO*)=NO*)(O*)O* Chemical compound *C(C(C(*)=NO*)=NO*)(O*)O* 0.000 description 1
- VOYADQIFGGIKAT-UHFFFAOYSA-N 1,3-dibutyl-4-hydroxy-2,6-dioxopyrimidine-5-carboximidamide Chemical compound CCCCn1c(O)c(C(N)=N)c(=O)n(CCCC)c1=O VOYADQIFGGIKAT-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 238000007098 aminolysis reaction Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical class ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- MVDYEFQVZNBPPH-UHFFFAOYSA-N pentane-2,3,4-trione Chemical compound CC(=O)C(=O)C(C)=O MVDYEFQVZNBPPH-UHFFFAOYSA-N 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19844919.4 | 1998-09-30 | ||
| DE19844919 | 1998-09-30 | ||
| PCT/EP1999/006862 WO2000018726A1 (de) | 1998-09-30 | 1999-09-16 | Verfahren zur herstellung von trion-bis(oximether) derivaten sowie damit erhältliche trion-mono- und trion-bis(oximether) derivate |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002525353A JP2002525353A (ja) | 2002-08-13 |
| JP2002525353A5 true JP2002525353A5 (OSRAM) | 2006-06-15 |
| JP4336046B2 JP4336046B2 (ja) | 2009-09-30 |
Family
ID=7882851
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000572188A Expired - Fee Related JP4336046B2 (ja) | 1998-09-30 | 1999-09-16 | トリオンビス（オキシムエーテル）誘導体の調製方法、およびそれによって得られるトリオンモノ−およびトリオンビス（オキシムエーテル）誘導体 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US6441236B1 (OSRAM) |
| EP (1) | EP1117636B1 (OSRAM) |
| JP (1) | JP4336046B2 (OSRAM) |
| KR (1) | KR100653800B1 (OSRAM) |
| CN (2) | CN1177814C (OSRAM) |
| AT (1) | ATE229500T1 (OSRAM) |
| AU (1) | AU6191599A (OSRAM) |
| BR (1) | BR9914205B1 (OSRAM) |
| CA (1) | CA2345717C (OSRAM) |
| CZ (1) | CZ300878B6 (OSRAM) |
| DE (1) | DE59903779D1 (OSRAM) |
| DK (1) | DK1117636T3 (OSRAM) |
| ES (1) | ES2189493T3 (OSRAM) |
| HU (1) | HUP0103458A3 (OSRAM) |
| IL (1) | IL141715A0 (OSRAM) |
| PL (1) | PL197555B1 (OSRAM) |
| PT (1) | PT1117636E (OSRAM) |
| WO (1) | WO2000018726A1 (OSRAM) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL152247A0 (en) * | 2000-04-11 | 2003-05-29 | Basf Ag | Method for producing oxime ethers |
| DK1296939T3 (da) * | 2000-07-05 | 2006-01-30 | Basf Ag | Fremgangsmåde til fremstilling af trioximderivater |
| CN103044283A (zh) * | 2012-09-07 | 2013-04-17 | 赵立地 | 一种制备肟醚的方法 |
| CN103524379B (zh) * | 2013-10-23 | 2015-04-15 | 江苏七洲绿色化工股份有限公司 | 一种肟菌酯的合成方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4435421A (en) | 1978-11-03 | 1984-03-06 | Union Carbide Corporation | Biocidal sulfur-containing bis-imino carbamate compounds |
| DE19539324A1 (de) * | 1995-10-23 | 1997-04-24 | Basf Ag | Phenylessigsäurederivate, Verfahren und Zwischenprodukte zu ihrer Herstellung und sie enthaltende Mittel |
| WO1998016499A1 (en) | 1996-10-15 | 1998-04-23 | Shionogi & Co., Ltd. | Oxime derivatives, hydrazone derivatives, and use thereof |
-
1999
- 1999-09-16 JP JP2000572188A patent/JP4336046B2/ja not_active Expired - Fee Related
- 1999-09-16 ES ES99948764T patent/ES2189493T3/es not_active Expired - Lifetime
- 1999-09-16 PT PT99948764T patent/PT1117636E/pt unknown
- 1999-09-16 CN CNB998116327A patent/CN1177814C/zh not_active Expired - Fee Related
- 1999-09-16 US US09/787,950 patent/US6441236B1/en not_active Expired - Lifetime
- 1999-09-16 HU HU0103458A patent/HUP0103458A3/hu unknown
- 1999-09-16 AT AT99948764T patent/ATE229500T1/de active
- 1999-09-16 CZ CZ20011016A patent/CZ300878B6/cs not_active IP Right Cessation
- 1999-09-16 AU AU61915/99A patent/AU6191599A/en not_active Abandoned
- 1999-09-16 CA CA002345717A patent/CA2345717C/en not_active Expired - Fee Related
- 1999-09-16 CN CNB2003101205369A patent/CN1256335C/zh not_active Expired - Fee Related
- 1999-09-16 IL IL14171599A patent/IL141715A0/xx not_active IP Right Cessation
- 1999-09-16 PL PL347059A patent/PL197555B1/pl not_active IP Right Cessation
- 1999-09-16 WO PCT/EP1999/006862 patent/WO2000018726A1/de not_active Ceased
- 1999-09-16 KR KR1020017004022A patent/KR100653800B1/ko not_active Expired - Fee Related
- 1999-09-16 DK DK99948764T patent/DK1117636T3/da active
- 1999-09-16 EP EP99948764A patent/EP1117636B1/de not_active Expired - Lifetime
- 1999-09-16 DE DE59903779T patent/DE59903779D1/de not_active Expired - Lifetime
- 1999-09-16 BR BRPI9914205-8B1A patent/BR9914205B1/pt not_active IP Right Cessation
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