JP6338599B2 - 2−オキソ−1,3−ジオキソラン−4−カルボキサミドのビルディングブロック、その製造及び使用 - Google Patents
2−オキソ−1,3−ジオキソラン−4−カルボキサミドのビルディングブロック、その製造及び使用 Download PDFInfo
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- JP6338599B2 JP6338599B2 JP2015555703A JP2015555703A JP6338599B2 JP 6338599 B2 JP6338599 B2 JP 6338599B2 JP 2015555703 A JP2015555703 A JP 2015555703A JP 2015555703 A JP2015555703 A JP 2015555703A JP 6338599 B2 JP6338599 B2 JP 6338599B2
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- Prior art keywords
- diisocyanate
- oxo
- dioxolane
- group
- carboxamide
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- INDZWIZFONXCIY-UHFFFAOYSA-N OC(C(CO1)OC1=O)=O Chemical compound OC(C(CO1)OC1=O)=O INDZWIZFONXCIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/32—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D317/34—Oxygen atoms
- C07D317/36—Alkylene carbonates; Substituted alkylene carbonates
- C07D317/38—Ethylene carbonate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polyurethanes Or Polyureas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Description
1H NMR (500 MHz, CDCl3): 3.82 (3H, s, CH3), 4.50 (1H, dd, J = 5.5, 9.0, CH2), 4.66 (1H, dd, J = 9.0, 9.0, CH2), 5.09 (1H, dd, J = 9.0, 5.5, CH);
13C NMR (125 MHz, CDCl3): 53.81 (CH3), 67.00 (CH2), 72.34 (CH), 153.97 (-O-CO-O-), 167.42 (-CO-O-);
IR (neat): 1812 cm-1 (-O-CO-O-), 1742 cm-1 (-CO-O-)。
1H-NMR (CDCl3/DMSO-d6 (1/0.1 [mol/mol])): 9.486 (broad, s; 1H); 5.012 (dd; 1H); 4.637 (t; 1H); 4.506 (dd; 1H);
13C-NMR (CDCl3/DMSO-d6 (1/0.1 [mol/ mol])): 168.425 (CO 酸); 153.348 (CO シクロカーボネート); 72.247 (CH-COOH); 66.988 (CH2CH-COOH);
IR (ν [cm-1]): 2977 bs (OH 酸), 2751 bw, 2658 bw, 2621 bw, 2538 bw, 2407 bw, 1785 bm (CO シクロカーボネート), 1793 bs (CO 酸), 1546 w, 1481 w, 1431 w, 1399 s, 1345 w, 1325 w, 128 m, 1196 s, 1087 s, 1074 s, 1039 m, 928 w, 832 s, 769 s, 724 m, 699 s, 650 m, 633 s, 525 s。
NCO含量: 11.66 % (理論値: 13.48 %);
1H-NMR (DMSO-d6): 8.35 (s, 1H, NH), 5.12 (dm, 1H, シクロカーボネート), 4.65 (m, 1H, シクロカーボネート), 4.39 (m, 1H, シクロカーボネート), 3.31 (m, 2H, CH2), 2.89 (m, 1H, CH), 1.61-0.70 (m, 15H, アルキル-CH2及び-CH3);
13C-NMR (DMSO-d6): 167.4 (CON), 165.9 (CON'), 154.4 (OC(O)O), 122.3 (NCO), 73.3 (CH-シクロカーボネート), 67.4 (CH2-シクロカーボネート), 52.2 (アルキル-CH2), 46.6 (アルキル-CH2), 44.8 (CH2-N), 42.2 (アルキル-CH2), 36.1 (CH-N), 34.8 (CH3), 31.3 (CH3), 27.3 (CH3), 25.1 (Cquart.-Me2), 22.9 (Cquart.-CH2-N) ppm;
IR (ν [cm-1]): 3316 (m, NH), 2954 (m), 2925 (m), 2874 (m), 2253 (s, NCO), 1812 (s, CO-シクロカーボネート), 1790 (s, CO-シクロカーボネート), 1671 (s, CO-アミド), 1546 (s, C-N), 1462 (w), 1366 (m), 1304 (w), 1241 (w), 1156 (s), 1062 (s), 895 (w), 857 (w), 767 (m), 729 (w), 577 (m), 470 (w), 432 (w)。
NCO-含量: 15.70 % (理論値: 16.02 %);
1H-NMR (DMSO-d6): 10.49 (s, 1H, NH), 7.52-7.11 (m, 3H, Ar), 5.27 (m, 1H, シクロカーボネート), 4.71 (m, 1H, シクロカーボネート), 4.55 (m, 1H, シクロカーボネート), 2.24 (m, 3H, CH3);
13C-NMR (THF-d8): 166.9 (NHC(O)O), 154.4 (OC(O)O), 138.2, 133.6, 131.5, 129.6 (Ar), 126.1 (NCO), 118.5, 117.5 (Ar), 74.6 (CH-シクロカーボネート), 68.0 (CH2-シクロカーボネート), 17.8 (CH3)。
DBTL(0.02質量%)の存在下で、実施例11又は12で得られた生成物を、ヘキサン−1,6−ジオールと反応させ、二官能性プレポリマーを得た。具体的には、当該生成物の5.0g(0.019mol)を乾燥THF中に溶解し、1.13gのヘキサン−1,6−ジオール(9.53mmol)及び1.2mgのDBTL(0.002mmol)を加えた。反応混合物を、4時間60℃で加熱した。溶媒の蒸発後、黄色〜茶色の粉末状の生成物が得られた。
1H-NMR (THF-d8): 7.79 (s, 1H, NH), 5.02 (m, 1H, シクロカーボネート), 4.65 (m, 1H, シクロカーボネート), 4.49 (m, 1H, シクロカーボネート), 3.87 (m, 6H, 3x CH2-N), 3.34 (t, 4H, 2x CH2-NCO), 3.26 (m, 2H, CH2-N-アミド), 1.67- 1.37 (m, 24H, 12 x CH2) ppm。
1H-NMR (THF-d8): 7.81 (s, 2H, NH), 5.05 (m, 2H, シクロカーボネート), 4.67 (m, 2H, シクロカーボネート), 4.50 (m, 2H, シクロカーボネート), 3.85 (m, 6H, 3x CH2-N), 3.34 (t, 2H, CH2-NCO), 3.26 (m, 4H, CH2-N-アミド), 1.67- 1.37 (m, 24H, 12 x CH2) ppm。
Claims (10)
- nは、2から3の整数である、請求項1に記載の2−オキソ−1,3−ジオキソラン−4−カルボキサミド。
- 前記ポリイソシアネートは、脂肪族ポリイソシアネート、芳香族ポリイソシアネート、又は脂肪族と芳香族とが組合わされたポリイソシアネートである、請求項1または2に記載の2−オキソ−1,3−ジオキソラン−4−カルボキサミド。
- 前記ポリイソシアネートは、テトラメチレン1,4−ジイソシアネート、2−メチルペンタメチレン1,5−ジイソシアネート、ヘキサメチレン1,6−ジイソシアネート(HDI)、2,2,4−及び2,4,4−トリメチルヘキサメチレン1,6−ジイソシアネート(TMDI)、ドデカメチレン1,12−ジイソシアネート、リシンジイソシアネート及びリシンエステルジイソシアネート、1−イソシアナト−3,3,5−トリメチル−5−イソシアナトメチルシクロヘキサン(イソホロンジイソシアネート−IPDI)、1,4−ジイソシアナト−2,2,6−トリメチルシクロへキサン(TMCDI)、2,2’−、2,4’−及び4,4’−ジシクロヘキシルメタンジイソシアネート(H12MDI)、シクロヘキサン1,3−ジイソシアネート及びシクロヘキサン1,4−ジイソシアネート(CHDI)、1,3−及び1,4−ビス(イソシアナトメチル)シクロヘキサン、4,4’−ジイソシアナトジシクロヘキシル−2,2−プロパン、m−及びp−フェニレンジイソシアネート、2,3,5,6−テトラメチル−1,4−ジイソシアナトベンゼン、3,3’−ジメチル−4,4’−ジイソシアナトジフェニル(TODI)、2,4−及び2,6−トルエンジイソシアネート(TDI)、2,2’−、2,4’−及び4,4’−ジフェニルメタンジイソシアネート(MDI)、ナフタレン1,2−ジイソシアネート及びナフタレン1,5−ジイソシアネート(NDI)、m−及びp−キシリレンジイソシアネート(XDI)、テトラメチルキシリレンジイソシアネート(TMXDI)、HDI三量体、ポリメリックMDI、並びにこれらの混合物から選択される、請求項1から3までのいずれか1項に記載の2−オキソ−1,3−ジオキソラン−4−カルボキサミド。
- 前記反応を、第三級アミン、有機金属化合物及びこれらの混合物から選択される触媒の存在下で行うことを特徴とする、請求項5に記載の方法。
- 前記触媒は、ジメチルシクロヘキシルアミン、4−ジメチルアミノピリジン(DMAP)、ジアザビシクロオクタン(DABCO)、ジアザビシクロウンデセン(DBU)、ジブチル錫ジラウレート(DBTL)、ビスマスカルボキシレート、チタン若しくはジルコニウムアルコキシレート又はカルボキシレート、並びにこれらの混合物から選択されることを特徴とする、請求項6に記載の方法。
- ビスマスカルボキシレートが、ビスマスオクタノエート又はビスマスネオデカノエートであることを特徴とする、請求項7に記載の方法。
- 2−オキソ−1,3−ジオキソラン−4−カルボキサミド置換されたプレポリマーの製造のための、請求項1から4までのいずれか1項に記載の2−オキソ−1,3−ジオキソラン−4−カルボキサミドの使用。
- 請求項9によって得られる、2−オキソ−1,3−ジオキソラン−4−カルボキサミド置換されたプレポリマー。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP13153383.8A EP2762471A1 (en) | 2013-01-31 | 2013-01-31 | 2-oxo-1,3-dioxolane-4-carboxamide building blocks, their preparation and use |
EP13153383.8 | 2013-01-31 | ||
PCT/EP2014/051784 WO2014118268A1 (en) | 2013-01-31 | 2014-01-30 | 2-oxo-1,3-dioxolane-4-carboxamide building blocks, their preparation and use |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2016508493A JP2016508493A (ja) | 2016-03-22 |
JP2016508493A5 JP2016508493A5 (ja) | 2017-03-02 |
JP6338599B2 true JP6338599B2 (ja) | 2018-06-06 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2015555703A Active JP6338599B2 (ja) | 2013-01-31 | 2014-01-30 | 2−オキソ−1,3−ジオキソラン−4−カルボキサミドのビルディングブロック、その製造及び使用 |
Country Status (12)
Country | Link |
---|---|
US (1) | US9617238B2 (ja) |
EP (2) | EP2762471A1 (ja) |
JP (1) | JP6338599B2 (ja) |
CN (1) | CN104918930B (ja) |
AU (1) | AU2014211407B2 (ja) |
BR (1) | BR112015014403B1 (ja) |
CA (1) | CA2896828C (ja) |
ES (1) | ES2792914T3 (ja) |
MX (1) | MX363692B (ja) |
RU (1) | RU2674343C2 (ja) |
SA (1) | SA515360761B1 (ja) |
WO (1) | WO2014118268A1 (ja) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2818465A1 (en) | 2013-06-26 | 2014-12-31 | Construction Research & Technology GmbH | 2-Oxo-1,3-dioxolane-4-acyl halides, their preparation and use |
EP2915808A1 (en) | 2014-03-07 | 2015-09-09 | Construction Research & Technology GmbH | 2-Hydroxyethyl 2-oxo-1,3-dioxolane-4-carboxylates, their preparation and use |
EP2998331A1 (en) * | 2014-09-17 | 2016-03-23 | Construction Research & Technology GmbH | A curable organic polymer comprising at least one acylurea unit, its preparation and use |
CN107072211B (zh) | 2014-11-07 | 2020-09-22 | 巴斯夫欧洲公司 | 含有2-氧代-1,3-二氧戊环-4羧酸酯的农业化学助剂 |
US11096248B2 (en) * | 2015-05-29 | 2021-08-17 | Watlow Electric Manufacturing Company | Resistive heater with temperature sensing power pins and auxiliary sensing junction |
CN107922569B (zh) * | 2015-08-10 | 2021-02-12 | 建筑研究和技术有限公司 | 用于制备开环聚合产物的方法 |
EP3464405A1 (de) * | 2016-06-03 | 2019-04-10 | Basf Se | Verwendung von verbindungen mit n 2-oxo-1,3-dioxolan-4-carbonsäureamid-einheiten in zweikomponentenklebstoffen |
KR102068311B1 (ko) * | 2017-09-13 | 2020-01-20 | 주식회사 엘지화학 | 경화성 조성물 |
KR102271847B1 (ko) * | 2017-09-13 | 2021-07-01 | 주식회사 엘지화학 | 경화성 조성물 |
FR3088326B1 (fr) * | 2018-11-09 | 2021-12-03 | Bostik Sa | Hydroxysilanes fonctionnalises, polyurethanes silyles, et compositions les comprenant |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
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IT1022442B (it) * | 1974-09-30 | 1978-03-20 | Montedison Spa | Procedimento per la preparazione di alchilencarbonati |
EP0001088A1 (de) | 1977-09-05 | 1979-03-21 | BASF Aktiengesellschaft | Carbonatgruppen enthaltende Polymerisate |
GB8921182D0 (en) * | 1989-09-19 | 1989-11-08 | Ici Plc | Novel chemical blowing agent |
JP3067319B2 (ja) * | 1991-10-07 | 2000-07-17 | 大日本インキ化学工業株式会社 | 水性硬化性樹脂組成物 |
JP3586881B2 (ja) | 1994-04-19 | 2004-11-10 | 三菱化学株式会社 | ジオキソラン含有溶剤 |
FR2784113B1 (fr) * | 1998-10-02 | 2002-06-07 | Rhodia Chimie Sa | Isocyanates modifies |
AU2003245663A1 (en) | 2002-06-28 | 2004-01-19 | Altus Biologics Inc. | Process for the enzymatic resolution of 1,3-dioxolane-4-carboxylates |
JP2006003433A (ja) | 2004-06-15 | 2006-01-05 | Sekisui Chem Co Ltd | 液晶表示素子用シール剤、上下導通材料及び液晶表示素子 |
EP1932840B1 (en) | 2005-10-03 | 2014-04-09 | Ono Pharmaceutical Co., Ltd. | Nitrogen-containing heterocyclic compound and pharmaceutical application thereof |
EP1941946A1 (en) | 2007-01-04 | 2008-07-09 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Carbonitrides as catalysts |
FR2914309B1 (fr) * | 2007-03-27 | 2011-07-08 | Rhodia Recherches & Tech | Composition a base de (poly)isocyanate modifie et d'un solvant de type acetal ou cetone aliphatique,et utilisation de cette composition pour la fabrication de revetements |
US8044194B2 (en) | 2009-06-12 | 2011-10-25 | International Business Machines Corporation | Cyclic carbonyl monomers functionalized with carbohydrates, polymers derived therefrom, and methods of preparation thereof |
US8742137B2 (en) | 2010-06-17 | 2014-06-03 | Construction Research & Technology Gmbh | 2-oxo-1, 3-dioxolane-4-carboxylic acid and derivatives thereof, their preparation and use |
EP2397474A1 (de) | 2010-06-17 | 2011-12-21 | Construction Research & Technology GmbH | 2-Oxo-1,3-dioxolan-4-carbonsäureester, ihre Herstellung und Verwendung |
WO2012065879A1 (en) | 2010-11-16 | 2012-05-24 | Basf Se | Process for the preparation of 2-oxo-[1,3] dioxolane-4-carboxylic acid esters |
ES2592631T3 (es) | 2011-12-22 | 2016-11-30 | Construction Research & Technology Gmbh | 2-Oxo-1,3-dioxolano-4-carboxamidas, su preparación y uso |
-
2013
- 2013-01-31 EP EP13153383.8A patent/EP2762471A1/en not_active Withdrawn
-
2014
- 2014-01-30 JP JP2015555703A patent/JP6338599B2/ja active Active
- 2014-01-30 ES ES14702016T patent/ES2792914T3/es active Active
- 2014-01-30 US US14/760,834 patent/US9617238B2/en active Active
- 2014-01-30 RU RU2015136648A patent/RU2674343C2/ru active
- 2014-01-30 EP EP14702016.8A patent/EP2951166B1/en active Active
- 2014-01-30 BR BR112015014403-9A patent/BR112015014403B1/pt active IP Right Grant
- 2014-01-30 WO PCT/EP2014/051784 patent/WO2014118268A1/en active Application Filing
- 2014-01-30 CN CN201480005232.4A patent/CN104918930B/zh active Active
- 2014-01-30 MX MX2015009852A patent/MX363692B/es unknown
- 2014-01-30 AU AU2014211407A patent/AU2014211407B2/en active Active
- 2014-01-30 CA CA2896828A patent/CA2896828C/en active Active
-
2015
- 2015-07-16 SA SA515360761A patent/SA515360761B1/ar unknown
Also Published As
Publication number | Publication date |
---|---|
MX2015009852A (es) | 2015-10-05 |
MX363692B (es) | 2019-03-29 |
US20150353521A1 (en) | 2015-12-10 |
EP2762471A1 (en) | 2014-08-06 |
SA515360761B1 (ar) | 2017-10-30 |
BR112015014403B1 (pt) | 2020-05-12 |
EP2951166B1 (en) | 2020-03-11 |
ES2792914T3 (es) | 2020-11-12 |
RU2015136648A (ru) | 2017-03-07 |
CA2896828A1 (en) | 2014-08-07 |
RU2674343C2 (ru) | 2018-12-07 |
JP2016508493A (ja) | 2016-03-22 |
BR112015014403A2 (pt) | 2017-08-22 |
CN104918930B (zh) | 2017-08-18 |
US9617238B2 (en) | 2017-04-11 |
CA2896828C (en) | 2021-04-06 |
EP2951166A1 (en) | 2015-12-09 |
AU2014211407A1 (en) | 2015-08-13 |
WO2014118268A1 (en) | 2014-08-07 |
CN104918930A (zh) | 2015-09-16 |
AU2014211407B2 (en) | 2017-09-21 |
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