NO328093B1 - Fremgangsmate for fremstilling av β-hydroksyalkylamider - Google Patents
Fremgangsmate for fremstilling av β-hydroksyalkylamider Download PDFInfo
- Publication number
- NO328093B1 NO328093B1 NO20015202A NO20015202A NO328093B1 NO 328093 B1 NO328093 B1 NO 328093B1 NO 20015202 A NO20015202 A NO 20015202A NO 20015202 A NO20015202 A NO 20015202A NO 328093 B1 NO328093 B1 NO 328093B1
- Authority
- NO
- Norway
- Prior art keywords
- general formula
- hydroxyalkylamides
- stated
- carboxylic acid
- alkanolamine
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims abstract 3
- 238000000034 method Methods 0.000 title claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 7
- 238000003756 stirring Methods 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 claims description 2
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 claims description 2
- 229940043276 diisopropanolamine Drugs 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000003431 cross linking reagent Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 238000007098 aminolysis reaction Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- -1 carboxylic acid halide Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/67—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/68—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/69—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom of an acyclic saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10053194A DE10053194A1 (de) | 2000-10-26 | 2000-10-26 | ß-Hydroxyalkylamide, Verfahren zu ihrer Herstellung und deren Verwendung |
Publications (3)
Publication Number | Publication Date |
---|---|
NO20015202D0 NO20015202D0 (no) | 2001-10-24 |
NO20015202L NO20015202L (no) | 2002-04-29 |
NO328093B1 true NO328093B1 (no) | 2009-12-07 |
Family
ID=7661187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20015202A NO328093B1 (no) | 2000-10-26 | 2001-10-24 | Fremgangsmate for fremstilling av β-hydroksyalkylamider |
Country Status (17)
Country | Link |
---|---|
US (2) | US20020055595A1 (fr) |
EP (1) | EP1203763B1 (fr) |
JP (1) | JP2002145839A (fr) |
KR (1) | KR100821024B1 (fr) |
CN (1) | CN1315785C (fr) |
AT (1) | ATE449063T1 (fr) |
AU (1) | AU784957B2 (fr) |
BR (1) | BR0104738A (fr) |
CA (1) | CA2359768C (fr) |
CZ (1) | CZ302774B6 (fr) |
DE (2) | DE10053194A1 (fr) |
ES (1) | ES2333643T3 (fr) |
MX (1) | MXPA01010682A (fr) |
NO (1) | NO328093B1 (fr) |
NZ (1) | NZ514573A (fr) |
PL (1) | PL204666B1 (fr) |
TW (1) | TW574183B (fr) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE555904T1 (de) | 2009-08-10 | 2012-05-15 | Eastman Kodak Co | Lithografische druckplattenvorläufer mit betahydroxy-alkylamid-vernetzern |
CN101704762B (zh) * | 2009-11-13 | 2013-01-09 | 六安市捷通达化工有限责任公司 | 一种β-羟烷基酰胺的生产工艺 |
JP6283477B2 (ja) * | 2012-06-25 | 2018-02-21 | ローム アンド ハース エレクトロニック マテリアルズ エルエルシーRohm and Haas Electronic Materials LLC | アミド成分を含むフォトレジスト |
CN103641737B (zh) * | 2013-11-29 | 2016-04-20 | 六安市捷通达化工有限责任公司 | 一种羧酸改性的羟烷基酰胺固化剂的制备方法 |
CN106986786A (zh) * | 2017-02-27 | 2017-07-28 | 沈阳化工大学 | 一种合成β‑羟烷基酰胺的工艺方法 |
BR112022003937A2 (pt) | 2019-09-03 | 2022-05-31 | Poliresin S R L | Polímero acrílico, polímero de hidroxialquilamida, processo para fabricar um polímero de hidroxialquilamida, uso do polímero, método para reticular polímeros e mistura de monômeros |
EP4299656A1 (fr) | 2022-07-01 | 2024-01-03 | Evonik Operations GmbH | Fabrication des amides propoxylés de l'acide benzènedicarboxylique et mousse polyuréthane correspondante |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH472364A (de) * | 1966-12-22 | 1969-05-15 | Geigy Ag J R | Verfahren zur Herstellung eines neuen polycyclischen Amins |
US3932324A (en) * | 1974-06-13 | 1976-01-13 | American Cyanamid Company | Light stabilizer compositions for polymers |
US4801680A (en) * | 1987-12-30 | 1989-01-31 | Ppg Industries, Inc. | Hydroxyalkylamide powder coating curing system |
US5101073A (en) * | 1990-08-27 | 1992-03-31 | Rohm And Haas Company | Production of β-hydroxyalkylamides |
US5506224A (en) * | 1991-12-31 | 1996-04-09 | Lifegroup S.P.A. | N-acyl derivatives of aminoalcohols active as local autacoids and useful in the therapy of autoimmune processes |
CN1057519C (zh) * | 1992-02-28 | 2000-10-18 | 罗姆和哈斯公司 | β-羟酰胺的制备 |
US5216090A (en) * | 1992-07-27 | 1993-06-01 | Rohm And Haas Company | Fatty acid hydroxyalkylamides as coreactable stabilizers and flow aids for powder coatings |
DE4230229A1 (de) * | 1992-09-10 | 1994-03-17 | Ge Polymertrend Gmbh | Beschichtungsmittel zur Beschichtung von Substraten aus thermoplastischem Kunststoff sowie Verfahren zum Aufbringen einer Schicht aus Pulverlack auf ein thermoplastisches Kunststoffsubstrat |
DE19823925C2 (de) * | 1998-05-28 | 2001-01-11 | Inventa Ag | Verfahren zur Herstellung von beta-Hydroxyalkylamiden |
-
2000
- 2000-10-26 DE DE10053194A patent/DE10053194A1/de not_active Ceased
-
2001
- 2001-07-20 US US09/909,573 patent/US20020055595A1/en not_active Abandoned
- 2001-09-24 AT AT01122856T patent/ATE449063T1/de not_active IP Right Cessation
- 2001-09-24 DE DE50115225T patent/DE50115225D1/de not_active Expired - Lifetime
- 2001-09-24 ES ES01122856T patent/ES2333643T3/es not_active Expired - Lifetime
- 2001-09-24 EP EP01122856A patent/EP1203763B1/fr not_active Expired - Lifetime
- 2001-09-26 CZ CZ20013461A patent/CZ302774B6/cs not_active IP Right Cessation
- 2001-09-26 AU AU76116/01A patent/AU784957B2/en not_active Ceased
- 2001-09-28 PL PL349933A patent/PL204666B1/pl unknown
- 2001-10-02 NZ NZ514573A patent/NZ514573A/xx not_active IP Right Cessation
- 2001-10-05 TW TW90124706A patent/TW574183B/zh not_active IP Right Cessation
- 2001-10-19 JP JP2001322105A patent/JP2002145839A/ja active Pending
- 2001-10-22 MX MXPA01010682A patent/MXPA01010682A/es active IP Right Grant
- 2001-10-23 CA CA2359768A patent/CA2359768C/fr not_active Expired - Lifetime
- 2001-10-24 NO NO20015202A patent/NO328093B1/no not_active IP Right Cessation
- 2001-10-24 BR BR0104738-8A patent/BR0104738A/pt not_active IP Right Cessation
- 2001-10-26 CN CNB011375140A patent/CN1315785C/zh not_active Expired - Fee Related
- 2001-10-26 KR KR1020010066270A patent/KR100821024B1/ko active IP Right Grant
-
2004
- 2004-06-12 US US10/866,979 patent/US7030272B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US7030272B2 (en) | 2006-04-18 |
CZ20013461A3 (cs) | 2002-06-12 |
KR100821024B1 (ko) | 2008-04-08 |
TW574183B (en) | 2004-02-01 |
KR20020032405A (ko) | 2002-05-03 |
CA2359768C (fr) | 2010-05-11 |
DE10053194A1 (de) | 2002-05-16 |
US20020055595A1 (en) | 2002-05-09 |
EP1203763A2 (fr) | 2002-05-08 |
EP1203763A3 (fr) | 2004-01-14 |
US20040260123A1 (en) | 2004-12-23 |
NO20015202D0 (no) | 2001-10-24 |
MXPA01010682A (es) | 2003-05-19 |
PL349933A1 (en) | 2002-05-06 |
AU7611601A (en) | 2002-05-02 |
EP1203763B1 (fr) | 2009-11-18 |
CN1315785C (zh) | 2007-05-16 |
DE50115225D1 (de) | 2009-12-31 |
NO20015202L (no) | 2002-04-29 |
ATE449063T1 (de) | 2009-12-15 |
ES2333643T3 (es) | 2010-02-25 |
CA2359768A1 (fr) | 2002-04-26 |
PL204666B1 (pl) | 2010-01-29 |
CN1351008A (zh) | 2002-05-29 |
JP2002145839A (ja) | 2002-05-22 |
BR0104738A (pt) | 2002-06-25 |
CZ302774B6 (cs) | 2011-11-02 |
AU784957B2 (en) | 2006-08-10 |
NZ514573A (en) | 2003-02-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO1999036369A1 (fr) | Utilisation d'un liant soluble dans l'eau pour la production de verre ou de laine de verre | |
JPH02294328A (ja) | ヒドロキシポリアミドの製法 | |
NO328093B1 (no) | Fremgangsmate for fremstilling av β-hydroksyalkylamider | |
JPS61140566A (ja) | ピペリジン誘導体、その製造方法およびこれを有効成分とする有機物質用安定剤 | |
JP6483481B2 (ja) | トルキシン酸系ポリマーおよびその製造中間体 | |
CN102531943B (zh) | 化合物及其制备方法 | |
KR100584037B1 (ko) | 치환된 아미도 프탈로시아닌 유도체의 제조방법 및 치환된 아미도 프탈로시아닌 유도체 | |
Zorić et al. | Ferrocene compounds. XXV. Synthesis and characterization of ferrocene‐containing oligoamides, their precursors, and analogues | |
WO2010101530A1 (fr) | Dérivés de silsesquioxane comportant des substituants contenant du soufre | |
US5925718A (en) | Process for preparing polyhydroxystyrene derivatives | |
JP2976057B2 (ja) | オクタキス(アルコキシフェニル)フタロシアニン系化合物およびその遷移金属錯体 | |
Ahn et al. | Zinc Acetate as a Catalyst for Di-and Triimide Formation from 1, 8-Naphthalic Anhydride and Aromatic Polyamines | |
JPH01149753A (ja) | ビス(ビフェニル)ジエステル誘導体およびその製造方法 | |
JPH04321643A (ja) | ジアセチレン含有安息香酸誘導体 | |
JPH09202756A (ja) | N−アリル置換メチルテトラヒドロフタル酸ハーフアミド化合物 | |
US5081219A (en) | Preparation of open chain poly(Reissert compounds) | |
JPH09202757A (ja) | N−アリル置換テトラヒドロフタル酸ハーフアミド化合物 | |
US5130469A (en) | Derivatives of n,n-bis(2,2-dimethyl-2-carboxy-ethyl)amine, manufacturing procedure and use of same | |
JP2002003482A (ja) | N−カルボキシ−t−ロイシン無水物の製造法 | |
JP2520298B2 (ja) | チオフェンジカルボン酸ジエステルの製造方法 | |
JPS6155A (ja) | 芳香族アミンの製造方法 | |
JPH09202758A (ja) | N−アリル置換トリメリット酸モノアミド化合物 | |
JPS63246369A (ja) | 2,3−ジオキソピペラジン類の製造法 | |
WO1997028117A1 (fr) | Nouveau procede pour fabriquer la l-glutamine et nouveaux intermediaires pour sa synthese | |
JPH0499757A (ja) | ジカルボン酸アミドエステルの製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM1K | Lapsed by not paying the annual fees |