CN101591331B - 一种受阻胺光稳定剂的制备方法 - Google Patents
一种受阻胺光稳定剂的制备方法 Download PDFInfo
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- CN101591331B CN101591331B CN200910074532.9A CN200910074532A CN101591331B CN 101591331 B CN101591331 B CN 101591331B CN 200910074532 A CN200910074532 A CN 200910074532A CN 101591331 B CN101591331 B CN 101591331B
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- 150000001412 amines Chemical class 0.000 title claims abstract description 21
- 239000004611 light stabiliser Substances 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 title abstract description 8
- 239000000243 solution Substances 0.000 claims abstract description 33
- 239000003960 organic solvent Substances 0.000 claims abstract description 15
- -1 piperidine diamine Chemical class 0.000 claims abstract description 6
- 238000006243 chemical reaction Methods 0.000 claims description 55
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 51
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 48
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 33
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 24
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 24
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 22
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 15
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 13
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 12
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- 239000003637 basic solution Substances 0.000 claims description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 10
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 10
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 10
- 239000007864 aqueous solution Substances 0.000 claims description 8
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 5
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 4
- 239000008096 xylene Substances 0.000 claims description 4
- 230000002209 hydrophobic effect Effects 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000003053 piperidines Chemical class 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 abstract description 11
- 238000007086 side reaction Methods 0.000 abstract description 6
- 239000012670 alkaline solution Substances 0.000 abstract description 5
- 230000035484 reaction time Effects 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract 3
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 abstract 1
- 238000007363 ring formation reaction Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 description 43
- 239000007787 solid Substances 0.000 description 28
- 238000001816 cooling Methods 0.000 description 21
- 238000010792 warming Methods 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 235000011121 sodium hydroxide Nutrition 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 11
- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 8
- 239000000706 filtrate Substances 0.000 description 7
- 238000001914 filtration Methods 0.000 description 7
- 229910017053 inorganic salt Inorganic materials 0.000 description 7
- 238000009413 insulation Methods 0.000 description 7
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
- 235000017550 sodium carbonate Nutrition 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 2
- FAKKRHFDVUQFFI-UHFFFAOYSA-N 1-N,1-N'-bis(2,2,6,6-tetramethylpiperidin-1-yl)hexane-1,1-diamine Chemical compound CCCCCC(NN1C(CCCC1(C)C)(C)C)NN2C(CCCC2(C)C)(C)C FAKKRHFDVUQFFI-UHFFFAOYSA-N 0.000 description 2
- QIJIUJYANDSEKG-UHFFFAOYSA-N 2,4,4-trimethylpentan-2-amine Chemical compound CC(C)(C)CC(C)(C)N QIJIUJYANDSEKG-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- NSOXQYCFHDMMGV-UHFFFAOYSA-N Tetrakis(2-hydroxypropyl)ethylenediamine Chemical compound CC(O)CN(CC(C)O)CCN(CC(C)O)CC(C)O NSOXQYCFHDMMGV-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- QVYARBLCAHCSFJ-UHFFFAOYSA-N butane-1,1-diamine Chemical compound CCCC(N)N QVYARBLCAHCSFJ-UHFFFAOYSA-N 0.000 description 2
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- SYECJBOWSGTPLU-UHFFFAOYSA-N hexane-1,1-diamine Chemical compound CCCCCC(N)N SYECJBOWSGTPLU-UHFFFAOYSA-N 0.000 description 2
- 229940094933 n-dodecane Drugs 0.000 description 2
- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical class [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
Abstract
Description
收率(%) | 平均分子量 | 溶解性 | |
实施例1 | 96.7 | 2450 | 好 |
实施例2 | 93 | 2250 | 好 |
实施例3 | 97 | 2560 | 好 |
实施例4 | 99.8 | 2380 | 好 |
实施例5 | 99.2 | 2430 | 好 |
实施例6 | 94 | 3450 | 好 |
实施例7 | 91 | 2870 | 好 |
Claims (2)
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CN200910074532.9A CN101591331B (zh) | 2009-06-25 | 2009-06-25 | 一种受阻胺光稳定剂的制备方法 |
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CN200910074532.9A CN101591331B (zh) | 2009-06-25 | 2009-06-25 | 一种受阻胺光稳定剂的制备方法 |
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CN101591331A CN101591331A (zh) | 2009-12-02 |
CN101591331B true CN101591331B (zh) | 2014-05-21 |
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Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
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CN102977367A (zh) * | 2012-11-29 | 2013-03-20 | 保定市乐凯化学有限公司 | 一种受阻胺光稳定剂的制备方法 |
CN105153120B (zh) * | 2015-10-19 | 2018-11-02 | 北京天罡助剂有限责任公司 | 一种低碱性受阻胺光稳定剂及其制备方法 |
CN105348525B (zh) * | 2015-10-19 | 2017-10-27 | 北京天罡助剂有限责任公司 | 一种低碱性聚合型受阻胺光稳定剂及其制备方法 |
CN105153121B (zh) * | 2015-10-20 | 2018-09-11 | 北京天罡助剂有限责任公司 | 受阻胺光稳定剂及其合成方法 |
KR102576757B1 (ko) * | 2016-08-29 | 2023-09-07 | 제이엔씨 주식회사 | 피페리딘 유도체, 액정 조성물, 및 액정 표시 소자 |
CN109575281B (zh) * | 2018-10-22 | 2020-12-18 | 保定市乐凯化学有限公司 | 受阻胺类光稳定剂的制备方法 |
CN109517108B (zh) * | 2018-10-22 | 2021-04-02 | 乐凯化学材料有限公司 | 制备马来酰亚胺/α-烯烃共聚物的方法 |
CN109456480A (zh) * | 2018-10-29 | 2019-03-12 | 北京天罡助剂有限责任公司 | 一种受阻胺光稳定剂及其制备方法 |
CN109251313A (zh) * | 2018-10-29 | 2019-01-22 | 北京天罡助剂有限责任公司 | 一种受阻胺光稳定剂及其制备方法 |
CN109265995A (zh) * | 2018-10-29 | 2019-01-25 | 北京天罡助剂有限责任公司 | 一种聚合型受阻胺光稳定剂及其应用 |
CN109503554B (zh) * | 2018-12-13 | 2020-10-30 | 天津利安隆新材料股份有限公司 | 一种聚合型受阻胺类光稳定剂ha-88的制备方法 |
CN112126060B (zh) * | 2019-06-25 | 2022-05-31 | 北京天罡助剂有限责任公司 | 一种聚合型高分子空间位阻胺及其制备方法 |
CN111303481B (zh) * | 2020-02-13 | 2021-09-03 | 西安工业大学 | 低聚合型受阻胺光稳定剂及其制备方法 |
CN112961405A (zh) * | 2021-02-09 | 2021-06-15 | 双键化工(上海)有限公司 | 一种用于聚烯烃木塑复合材料的高耐候性光稳定剂及复合光稳定剂 |
CN114507216A (zh) * | 2022-03-08 | 2022-05-17 | 河南省化工研究所有限责任公司 | 一种受阻胺类光稳定剂944的制备方法 |
CN115724828A (zh) * | 2022-11-23 | 2023-03-03 | 宿迁联盛助剂有限公司 | 一种低分布光稳定剂944的制备方法 |
CN115975189A (zh) * | 2022-12-26 | 2023-04-18 | 江苏富比亚化学品有限公司 | 一种受阻胺光稳定剂944的合成方法 |
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IT1195277B (it) * | 1981-10-02 | 1988-10-12 | Chimosa Chimica Organica Spa | Piperidil derivati di composti triazinici macrociclici,aventi attivita' stabilizzante per i polimeri e processi per la loro preparazione |
ITMI20012598A1 (it) * | 2001-12-11 | 2003-06-11 | 3V Sigma Spa | Hals macromolecolari a peso molecolare definito |
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2009
- 2009-06-25 CN CN200910074532.9A patent/CN101591331B/zh active Active
Non-Patent Citations (1)
Title |
---|
董传明等.受阻胺类光稳定剂Chima ssorb 2020的合成.《精细化工》.2005,第22卷(第6期),468-471,474. * |
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Address after: 071054, 6 Kennan Avenue, Baoding, Hebei Patentee after: CHINA LUCKY Group Corp. Patentee after: BAODING LUCKY CHEMICAL Co.,Ltd. Address before: 071054, 6 Kennan Avenue, Baoding, Hebei Patentee before: CHINA LUCKY FILM Group Corp. Patentee before: BAODING LUCKY CHEMICAL Co.,Ltd. |
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Effective date of registration: 20231024 Address after: 071054, 6 Kennan Avenue, Baoding, Hebei Patentee after: CHINA LUCKY Group Corp. Patentee after: Lucky chemical materials Co.,Ltd. Address before: 071054, 6 Kennan Avenue, Baoding, Hebei Patentee before: CHINA LUCKY Group Corp. Patentee before: BAODING LUCKY CHEMICAL Co.,Ltd. |