JP2007508322A5 - - Google Patents
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- Publication number
- JP2007508322A5 JP2007508322A5 JP2006534441A JP2006534441A JP2007508322A5 JP 2007508322 A5 JP2007508322 A5 JP 2007508322A5 JP 2006534441 A JP2006534441 A JP 2006534441A JP 2006534441 A JP2006534441 A JP 2006534441A JP 2007508322 A5 JP2007508322 A5 JP 2007508322A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl
- alkynyl
- alkenyl
- aryl
- 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.)
- Abandoned
Links
- -1 amide acetal Chemical class 0.000 claims description 33
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 17
- 239000008199 coating composition Substances 0.000 claims description 17
- 125000003342 alkenyl group Chemical group 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 125000000304 alkynyl group Chemical group 0.000 claims description 14
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 14
- 125000003118 aryl group Chemical group 0.000 claims description 14
- 150000002825 nitriles Chemical class 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 125000005907 alkyl ester group Chemical group 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- JIPSYSDANIXADL-UHFFFAOYSA-N [ethoxycarbonyl(isocyanato)amino] 2-methylprop-2-enoate Chemical compound CCOC(=O)N(OC(=O)C(C)=C)N=C=O JIPSYSDANIXADL-UHFFFAOYSA-N 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000003282 alkyl amino group Chemical group 0.000 claims description 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 6
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 6
- 125000001475 halogen functional group Chemical group 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- 229910000077 silane Inorganic materials 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 5
- 238000004132 cross linking Methods 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- 239000011701 zinc Substances 0.000 claims description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- 229910052793 cadmium Inorganic materials 0.000 claims description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 239000011651 chromium Substances 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 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 description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 150000003839 salts Chemical group 0.000 claims description 2
- 229910052706 scandium Inorganic materials 0.000 claims description 2
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 claims description 2
- 239000010936 titanium Substances 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000012948 isocyanate Substances 0.000 description 5
- 150000002513 isocyanates Chemical class 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 2
- 150000002118 epoxides Chemical class 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical group O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- 239000004971 Cross linker Substances 0.000 description 1
- VXCUURYYWGCLIH-UHFFFAOYSA-N Dodecanenitrile Chemical compound CCCCCCCCCCCC#N VXCUURYYWGCLIH-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical group OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- SZKKNEOUHLFYNA-UHFFFAOYSA-N undecanenitrile Chemical group CCCCCCCCCCC#N SZKKNEOUHLFYNA-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US50988503P | 2003-10-09 | 2003-10-09 | |
| PCT/US2004/033437 WO2005035613A1 (en) | 2003-10-09 | 2004-10-08 | Process for making amide acetals |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007508322A JP2007508322A (ja) | 2007-04-05 |
| JP2007508322A5 true JP2007508322A5 (cg-RX-API-DMAC7.html) | 2007-10-11 |
Family
ID=34435035
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006534441A Abandoned JP2007508322A (ja) | 2003-10-09 | 2004-10-08 | アミドアセタールの製造方法 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US7230112B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1670840B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2007508322A (cg-RX-API-DMAC7.html) |
| KR (1) | KR20060121907A (cg-RX-API-DMAC7.html) |
| CN (1) | CN1863835A (cg-RX-API-DMAC7.html) |
| AT (1) | ATE407162T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU2004280632A1 (cg-RX-API-DMAC7.html) |
| BR (1) | BRPI0415332A (cg-RX-API-DMAC7.html) |
| CA (1) | CA2541086C (cg-RX-API-DMAC7.html) |
| DE (1) | DE602004016358D1 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2311865T3 (cg-RX-API-DMAC7.html) |
| RU (1) | RU2006115580A (cg-RX-API-DMAC7.html) |
| WO (1) | WO2005035613A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2004227417A1 (en) * | 2003-04-04 | 2004-10-21 | E.I. Dupont De Nemours And Company | Polymeric crosslinkable compositions containing acetal amides |
| EP1805185A1 (en) * | 2004-09-30 | 2007-07-11 | E.I. Dupont De Nemours And Company | Hydroxy amide acetals and their use in coatings |
| US7608645B2 (en) | 2004-09-30 | 2009-10-27 | E.I. Du Pont De Nemours And Company | Dual cure coating compositions |
| CN101044178A (zh) * | 2004-09-30 | 2007-09-26 | 纳幕尔杜邦公司 | 涂料中的甲基丙烯酸酯酰胺缩醛 |
| JP2008514727A (ja) * | 2004-09-30 | 2008-05-08 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | コーティングでのポリマー／オリゴマーメタクリレート官能化アミドアセタール |
| JP2008514803A (ja) * | 2004-09-30 | 2008-05-08 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | コーティングでのメタクリレートアミドアセタール |
| US7504440B2 (en) * | 2004-09-30 | 2009-03-17 | E.I. Du Pont De Nemours & Company | Poly(meth)acrylate compositions containing amide acetals |
| CN101243114B (zh) | 2005-08-17 | 2012-05-23 | 阿克佐诺贝尔国际涂料股份有限公司 | 包含多异氰酸酯和多元醇的涂料组合物 |
| US7812173B2 (en) * | 2005-08-23 | 2010-10-12 | E.I. Du Pont De Nemours And Company | Tetrahydro-1,8-dioxa-4a-aza-naphthalenes in coating applications |
| US20070049752A1 (en) * | 2005-08-23 | 2007-03-01 | Drysdale Neville E | Preparation of 2,6-dioxa-7-aza-bicyclo[2.2.2] octanes |
| RU2510973C2 (ru) | 2008-10-22 | 2014-04-10 | Акцо Нобель Коатингс Интернэшнл Б.В. | Покрывная композиция, включающая полиизоцианат и полиол |
| EP2414416A1 (en) | 2009-03-31 | 2012-02-08 | Akzo Nobel Coatings International B.V. | Radiation curing of coatings |
| CN104136474B (zh) | 2012-03-07 | 2016-06-22 | 阿克佐诺贝尔国际涂料股份有限公司 | 非水性液体涂料组合物 |
| WO2014192314A1 (ja) | 2013-05-31 | 2014-12-04 | 凸版印刷株式会社 | 転写用積層媒体および印刷物 |
| JP6683136B2 (ja) | 2015-02-03 | 2020-04-15 | 凸版印刷株式会社 | 光学情報媒体 |
| WO2017199982A1 (ja) | 2016-05-16 | 2017-11-23 | 凸版印刷株式会社 | 光学情報媒体及びその製造方法 |
| US11780804B2 (en) | 2019-05-24 | 2023-10-10 | Ascend Performance Materials Operations Llc | Tricyanohexane purification methods |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1720361A1 (de) | 1967-01-31 | 1971-07-08 | Huels Chemische Werke Ag | Verfahren zur Herstellung linearer Polyesteramide |
| CA1249590A (en) | 1984-09-16 | 1989-01-31 | Anil B. Goel | Bicyclic amide acetal production |
| US4652655A (en) * | 1985-05-20 | 1987-03-24 | Ashland Oil, Inc. | Bicyclic amide acetals are prepared from organic nitriles and dialkanol amines at below about 140° C. and product is isolated by solvent extraction |
| US4636558A (en) * | 1985-12-16 | 1987-01-13 | Ashland Oil, Inc. | Polymer from bicyclic amide acetal-epoxide monomer and dicarboxylic acid anhydride |
| US4760178A (en) * | 1986-04-11 | 1988-07-26 | Ashland Oil, Inc. | Reactions of bicyclic amide acetals with ureas |
| ATE56016T1 (de) | 1986-11-17 | 1990-09-15 | Ashland Oil Inc | Verfahren zur herstellung von bicyclischen amidacetalen. |
| US4721767A (en) * | 1987-01-20 | 1988-01-26 | Ashland Oil, Inc. | Process for copolymerization of bicyclic amide acetals and polyisocyanates |
| NL1002427C2 (nl) | 1996-02-23 | 1997-08-26 | Akzo Nobel Nv | Bekledingssamenstelling omvattende een bicyclo- of spiroorthoester functionele verbinding. |
| AU2004227417A1 (en) | 2003-04-04 | 2004-10-21 | E.I. Dupont De Nemours And Company | Polymeric crosslinkable compositions containing acetal amides |
-
2004
- 2004-10-07 US US10/960,656 patent/US7230112B2/en not_active Expired - Lifetime
- 2004-10-08 JP JP2006534441A patent/JP2007508322A/ja not_active Abandoned
- 2004-10-08 DE DE602004016358T patent/DE602004016358D1/de not_active Expired - Lifetime
- 2004-10-08 AU AU2004280632A patent/AU2004280632A1/en not_active Abandoned
- 2004-10-08 KR KR1020067006747A patent/KR20060121907A/ko not_active Withdrawn
- 2004-10-08 AT AT04794710T patent/ATE407162T1/de not_active IP Right Cessation
- 2004-10-08 CA CA2541086A patent/CA2541086C/en not_active Expired - Fee Related
- 2004-10-08 EP EP04794710A patent/EP1670840B1/en not_active Expired - Lifetime
- 2004-10-08 CN CNA2004800295680A patent/CN1863835A/zh active Pending
- 2004-10-08 BR BRPI0415332-4A patent/BRPI0415332A/pt not_active IP Right Cessation
- 2004-10-08 RU RU2006115580/04A patent/RU2006115580A/ru not_active Application Discontinuation
- 2004-10-08 ES ES04794710T patent/ES2311865T3/es not_active Expired - Lifetime
- 2004-10-08 WO PCT/US2004/033437 patent/WO2005035613A1/en not_active Ceased
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