GB1409967A - Method for preparation of polymers containing aromatic amino groups in the side chain - Google Patents
Method for preparation of polymers containing aromatic amino groups in the side chainInfo
- Publication number
- GB1409967A GB1409967A GB3742673A GB3742673A GB1409967A GB 1409967 A GB1409967 A GB 1409967A GB 3742673 A GB3742673 A GB 3742673A GB 3742673 A GB3742673 A GB 3742673A GB 1409967 A GB1409967 A GB 1409967A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methacrylate
- polymer
- ethyl
- aromatic amino
- polymers
- 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.)
- Expired
Links
- 229920000642 polymer Polymers 0.000 title abstract 8
- 125000003118 aryl group Chemical group 0.000 title abstract 5
- 125000003277 amino group Chemical group 0.000 title abstract 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 239000000178 monomer Substances 0.000 abstract 3
- -1 sulphonyl group Chemical group 0.000 abstract 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 2
- MECSEIRTZGJPSN-UHFFFAOYSA-N (3-acetamidophenyl) 2-methylprop-2-enoate Chemical compound C(C(=C)C)(=O)OC1=CC(=CC=C1)NC(=O)C MECSEIRTZGJPSN-UHFFFAOYSA-N 0.000 abstract 1
- PZJZQKCKFRXTMP-UHFFFAOYSA-N (4-acetamidophenyl) 2-methylprop-2-enoate Chemical compound CC(=O)NC1=CC=C(OC(=O)C(C)=C)C=C1 PZJZQKCKFRXTMP-UHFFFAOYSA-N 0.000 abstract 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 abstract 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2,2'-azo-bis-isobutyronitrile Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 abstract 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 150000001450 anions Chemical group 0.000 abstract 1
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 abstract 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 abstract 1
- 230000008030 elimination Effects 0.000 abstract 1
- 238000003379 elimination reaction Methods 0.000 abstract 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 239000011148 porous material Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS574172A CS166317B1 (enrdf_load_html_response) | 1972-08-18 | 1972-08-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1409967A true GB1409967A (en) | 1975-10-15 |
Family
ID=5402868
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3742673A Expired GB1409967A (en) | 1972-08-18 | 1973-08-07 | Method for preparation of polymers containing aromatic amino groups in the side chain |
Country Status (12)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000044800A1 (en) * | 1999-01-29 | 2000-08-03 | Amersham Pharmacia Biotech K.K. | Temperature-responsive polymer compound and process for producing the same |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5160135A (en) * | 1987-12-11 | 1992-11-03 | Hasegawa Kagaku Kogyo Kabushiki Kaisha | Stick |
-
1972
- 1972-08-18 CS CS574172A patent/CS166317B1/cs unknown
-
1973
- 1973-07-31 BE BE134060A patent/BE803022A/xx unknown
- 1973-08-06 JP JP8768973A patent/JPS49132178A/ja active Pending
- 1973-08-07 GB GB3742673A patent/GB1409967A/en not_active Expired
- 1973-08-07 CA CA178,267A patent/CA1026497A/en not_active Expired
- 1973-08-07 DE DE19732339915 patent/DE2339915A1/de active Pending
- 1973-08-08 SE SE7310882A patent/SE388204B/xx unknown
- 1973-08-08 NL NL7310961A patent/NL7310961A/xx not_active Application Discontinuation
- 1973-08-09 AU AU59072/73A patent/AU468503B2/en not_active Expired
- 1973-08-14 AT AT712773A patent/AT339043B/de not_active IP Right Cessation
- 1973-08-15 CH CH1177573A patent/CH593999A5/xx not_active IP Right Cessation
- 1973-08-17 FR FR7330015A patent/FR2196349B1/fr not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000044800A1 (en) * | 1999-01-29 | 2000-08-03 | Amersham Pharmacia Biotech K.K. | Temperature-responsive polymer compound and process for producing the same |
| AU781633B2 (en) * | 1999-01-29 | 2005-06-02 | Ge Healthcare Bio-Sciences Kk | Temperature-responsive polymer compound and process for producing the same |
| US6956077B1 (en) | 1999-01-29 | 2005-10-18 | Amersham Biosciences Kk | Temperature-responsive polymer compound and process for producing the same |
Also Published As
| Publication number | Publication date |
|---|---|
| CS166317B1 (enrdf_load_html_response) | 1976-02-27 |
| AU468503B2 (en) | 1976-01-15 |
| ATA712773A (de) | 1977-01-15 |
| JPS49132178A (enrdf_load_html_response) | 1974-12-18 |
| AT339043B (de) | 1977-09-26 |
| AU5907273A (en) | 1975-02-13 |
| SE388204B (sv) | 1976-09-27 |
| DE2339915A1 (de) | 1974-02-28 |
| CA1026497A (en) | 1978-02-14 |
| BE803022A (fr) | 1973-11-16 |
| FR2196349A1 (enrdf_load_html_response) | 1974-03-15 |
| FR2196349B1 (enrdf_load_html_response) | 1978-01-27 |
| CH593999A5 (enrdf_load_html_response) | 1977-12-30 |
| NL7310961A (enrdf_load_html_response) | 1974-02-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |