CN106565513B - 利用微波加热制备β-羟烷基酰胺的方法 - Google Patents
利用微波加热制备β-羟烷基酰胺的方法 Download PDFInfo
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- CN106565513B CN106565513B CN201610886248.1A CN201610886248A CN106565513B CN 106565513 B CN106565513 B CN 106565513B CN 201610886248 A CN201610886248 A CN 201610886248A CN 106565513 B CN106565513 B CN 106565513B
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- microwave heating
- necked flask
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- microwave
- ester
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- 238000010438 heat treatment Methods 0.000 title claims abstract description 51
- 238000000034 method Methods 0.000 title claims abstract description 26
- 150000002148 esters Chemical class 0.000 claims abstract description 11
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229940043237 diethanolamine Drugs 0.000 claims abstract description 10
- 238000003756 stirring Methods 0.000 claims abstract description 10
- 239000003054 catalyst Substances 0.000 claims abstract description 8
- 238000002425 crystallisation Methods 0.000 claims abstract description 7
- 230000008025 crystallization Effects 0.000 claims abstract description 7
- 239000007787 solid Substances 0.000 claims abstract description 7
- 239000002798 polar solvent Substances 0.000 claims abstract description 5
- 238000009434 installation Methods 0.000 claims abstract description 3
- 238000006243 chemical reaction Methods 0.000 claims description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 12
- 239000002904 solvent Substances 0.000 claims description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 5
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical group [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims description 4
- UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical group COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 claims description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
- ALOUNLDAKADEEB-UHFFFAOYSA-N dimethyl sebacate Chemical compound COC(=O)CCCCCCCCC(=O)OC ALOUNLDAKADEEB-UHFFFAOYSA-N 0.000 claims description 3
- 239000000376 reactant Substances 0.000 claims description 3
- XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 claims description 2
- AJFDBNQQDYLMJN-UHFFFAOYSA-N n,n-diethylacetamide Chemical compound CCN(CC)C(C)=O AJFDBNQQDYLMJN-UHFFFAOYSA-N 0.000 claims description 2
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 claims description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- 229940014772 dimethyl sebacate Drugs 0.000 claims 1
- XHEDLZYGAQSNTR-UHFFFAOYSA-N ethene;hexanedioic acid Chemical compound C=C.C=C.OC(=O)CCCCC(O)=O XHEDLZYGAQSNTR-UHFFFAOYSA-N 0.000 claims 1
- -1 hydroxyalkyl amide Chemical class 0.000 abstract description 23
- 238000007086 side reaction Methods 0.000 abstract description 4
- 230000035484 reaction time Effects 0.000 abstract 1
- 230000005855 radiation Effects 0.000 description 5
- 150000001408 amides Chemical class 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- 230000029052 metamorphosis Effects 0.000 description 2
- OKRNLSUTBJUVKA-UHFFFAOYSA-N n,n,n',n'-Tetrakis(2-hydroxyethyl)adipamide Chemical compound OCCN(CCO)C(=O)CCCCC(=O)N(CCO)CCO OKRNLSUTBJUVKA-UHFFFAOYSA-N 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- OUPZKGBUJRBPGC-UHFFFAOYSA-N 1,3,5-tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound O=C1N(CC2OC2)C(=O)N(CC2OC2)C(=O)N1CC1CO1 OUPZKGBUJRBPGC-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- YWOITFUKFOYODT-UHFFFAOYSA-N methanol;sodium Chemical group [Na].OC YWOITFUKFOYODT-UHFFFAOYSA-N 0.000 description 1
- UUCAVBDCVCFNIN-UHFFFAOYSA-N n,n,n',n'-tetrakis(2-hydroxypropyl)hexanediamide Chemical compound CC(O)CN(CC(C)O)C(=O)CCCCC(=O)N(CC(C)O)CC(C)O UUCAVBDCVCFNIN-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
- 239000012855 volatile organic compound Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/02—Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (1)
Priority Applications (1)
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CN201610886248.1A CN106565513B (zh) | 2016-10-11 | 2016-10-11 | 利用微波加热制备β-羟烷基酰胺的方法 |
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CN201610886248.1A CN106565513B (zh) | 2016-10-11 | 2016-10-11 | 利用微波加热制备β-羟烷基酰胺的方法 |
Publications (2)
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CN106565513A CN106565513A (zh) | 2017-04-19 |
CN106565513B true CN106565513B (zh) | 2019-03-15 |
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CN201610886248.1A Expired - Fee Related CN106565513B (zh) | 2016-10-11 | 2016-10-11 | 利用微波加热制备β-羟烷基酰胺的方法 |
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CN (1) | CN106565513B (zh) |
Families Citing this family (2)
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CN110642742A (zh) * | 2019-09-18 | 2020-01-03 | 甘肃青宇新材料有限公司 | 一种β-羟烷基酰胺固化剂的制备方法 |
CN113583651B (zh) * | 2021-08-24 | 2022-05-20 | 四川冠山科技有限公司 | 耐高温清洁压裂稠化剂及其制备方法,应用,耐高温清洁压裂液 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1237576A (zh) * | 1998-05-28 | 1999-12-08 | 埃姆斯化学公司 | β-羟基烷基酰胺的制备方法 |
WO2009121485A1 (de) * | 2008-04-04 | 2009-10-08 | Clariant International Ltd | Kontinuierliches verfahren zur herstellung von fettsäurealkanolamiden |
CN101580478A (zh) * | 2009-06-17 | 2009-11-18 | 武汉工程大学 | 一种用微波合成三方向树形分子核的方法 |
CN101704762A (zh) * | 2009-11-13 | 2010-05-12 | 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 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
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DE102009031058A1 (de) * | 2009-06-30 | 2011-01-27 | Clariant International Ltd. | Kontinuierliches Verfahren zur Herstellung von Amiden aromatischer Carbonsäuren |
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- 2016-10-11 CN CN201610886248.1A patent/CN106565513B/zh not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1237576A (zh) * | 1998-05-28 | 1999-12-08 | 埃姆斯化学公司 | β-羟基烷基酰胺的制备方法 |
WO2009121485A1 (de) * | 2008-04-04 | 2009-10-08 | Clariant International Ltd | Kontinuierliches verfahren zur herstellung von fettsäurealkanolamiden |
CN101580478A (zh) * | 2009-06-17 | 2009-11-18 | 武汉工程大学 | 一种用微波合成三方向树形分子核的方法 |
CN101704762A (zh) * | 2009-11-13 | 2010-05-12 | 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 |
Non-Patent Citations (1)
Title |
---|
N,N,N’,N’-四(β-羟乙基)己二酰胺的合成工艺的研究;杨志萍等;《中国涂料》;20151031;第30卷(第10期);第48-50页 |
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