CN101121668B - 4,4’-二甲基三苯胺的合成方法 - Google Patents
4,4’-二甲基三苯胺的合成方法 Download PDFInfo
- Publication number
- CN101121668B CN101121668B CN2007101395431A CN200710139543A CN101121668B CN 101121668 B CN101121668 B CN 101121668B CN 2007101395431 A CN2007101395431 A CN 2007101395431A CN 200710139543 A CN200710139543 A CN 200710139543A CN 101121668 B CN101121668 B CN 101121668B
- Authority
- CN
- China
- Prior art keywords
- dimethyl
- reaction
- triphenylamine
- synthetic method
- bromobenzene
- 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 - Fee Related
Links
- YWKKLBATUCJUHI-UHFFFAOYSA-N 4-methyl-n-(4-methylphenyl)-n-phenylaniline Chemical compound C1=CC(C)=CC=C1N(C=1C=CC(C)=CC=1)C1=CC=CC=C1 YWKKLBATUCJUHI-UHFFFAOYSA-N 0.000 title claims abstract description 13
- 238000010189 synthetic method Methods 0.000 title claims description 10
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000002904 solvent Substances 0.000 claims abstract description 13
- 230000035484 reaction time Effects 0.000 claims abstract description 12
- 239000002994 raw material Substances 0.000 claims abstract description 10
- 230000005855 radiation Effects 0.000 claims abstract description 6
- 239000002253 acid Substances 0.000 claims abstract description 3
- 238000006243 chemical reaction Methods 0.000 claims description 40
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 claims description 22
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 3
- 239000011230 binding agent Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 5
- 239000003153 chemical reaction reagent Substances 0.000 abstract description 3
- 238000010438 heat treatment Methods 0.000 abstract description 3
- 238000001308 synthesis method Methods 0.000 abstract 2
- XAEBTCPOZVEMHR-UHFFFAOYSA-N 2-methylpropan-2-ol;potassium Chemical compound [K].CC(C)(C)O XAEBTCPOZVEMHR-UHFFFAOYSA-N 0.000 abstract 1
- RHPVVNRNAHRJOQ-UHFFFAOYSA-N 4-methyl-n-(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1NC1=CC=C(C)C=C1 RHPVVNRNAHRJOQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000004799 bromophenyl group Chemical group 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000000047 product Substances 0.000 description 10
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 9
- 239000003513 alkali Substances 0.000 description 8
- -1 polyoxyethylene Polymers 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 125000006617 triphenylamine group Chemical group 0.000 description 7
- YCOXTKKNXUZSKD-UHFFFAOYSA-N as-o-xylenol Natural products CC1=CC=C(O)C=C1C YCOXTKKNXUZSKD-UHFFFAOYSA-N 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- SNHMUERNLJLMHN-UHFFFAOYSA-N iodobenzene Chemical compound IC1=CC=CC=C1 SNHMUERNLJLMHN-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000013078 crystal Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000003444 phase transfer catalyst Substances 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 238000006887 Ullmann reaction Methods 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 239000000543 intermediate Substances 0.000 description 4
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 4
- 239000012074 organic phase Substances 0.000 description 4
- 238000001953 recrystallisation Methods 0.000 description 4
- 230000001988 toxicity Effects 0.000 description 4
- 231100000419 toxicity Toxicity 0.000 description 4
- 238000005303 weighing Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N pentanoic acid group Chemical group C(CCCC)(=O)O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 150000003983 crown ethers Chemical class 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- ITJSVDCZHCYXQE-UHFFFAOYSA-N toluene;hydroiodide Chemical compound I.CC1=CC=CC=C1 ITJSVDCZHCYXQE-UHFFFAOYSA-N 0.000 description 2
- OIRHKGBNGGSCGS-UHFFFAOYSA-N 1-bromo-2-iodobenzene Chemical compound BrC1=CC=CC=C1I OIRHKGBNGGSCGS-UHFFFAOYSA-N 0.000 description 1
- KLYCPFXDDDMZNQ-UHFFFAOYSA-N Benzyne Chemical compound C1=CC#CC=C1 KLYCPFXDDDMZNQ-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- YSGZPEILUZVKDO-UHFFFAOYSA-N [F].C1(=CC=CC=C1)N(C1=CC=CC=C1)C1=CC=CC=C1 Chemical group [F].C1(=CC=CC=C1)N(C1=CC=CC=C1)C1=CC=CC=C1 YSGZPEILUZVKDO-UHFFFAOYSA-N 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000005525 hole transport Effects 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 238000007648 laser printing Methods 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 150000005217 methyl ethers Chemical class 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 229960004839 potassium iodide Drugs 0.000 description 1
- 235000007715 potassium iodide Nutrition 0.000 description 1
- 125000001453 quaternary ammonium group Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
Claims (2)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2007101395431A CN101121668B (zh) | 2007-09-28 | 2007-09-28 | 4,4’-二甲基三苯胺的合成方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2007101395431A CN101121668B (zh) | 2007-09-28 | 2007-09-28 | 4,4’-二甲基三苯胺的合成方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101121668A CN101121668A (zh) | 2008-02-13 |
CN101121668B true CN101121668B (zh) | 2011-01-19 |
Family
ID=39084190
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2007101395431A Expired - Fee Related CN101121668B (zh) | 2007-09-28 | 2007-09-28 | 4,4’-二甲基三苯胺的合成方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN101121668B (zh) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104478737B (zh) * | 2014-11-22 | 2017-01-18 | 陈定奔 | 一种利用氨水为原料制备芳伯胺的合成方法 |
CN107043328A (zh) * | 2017-01-20 | 2017-08-15 | 上海巧坤化工科技有限公司 | 一种合成三苯基胺类化合物的新方法 |
CN109054044A (zh) * | 2018-09-26 | 2018-12-21 | 中国科学技术大学苏州研究院 | 一种多孔晶态材料及其制备方法和用途 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000239235A (ja) * | 1998-12-25 | 2000-09-05 | Hodogaya Chem Co Ltd | トリアリールアミン誘導体の製造方法 |
DE10002561A1 (de) * | 2000-01-19 | 2001-07-26 | Syntec Ges Fuer Chemie Und Tec | Verfahren zur Herstellung von Arylaminen |
DE19963009A1 (de) * | 1999-12-22 | 2001-08-09 | Syntec Ges Fuer Chemie Und Tec | Verfahren zur Herstellung von Arylaminen |
CN101012171A (zh) * | 2007-02-02 | 2007-08-08 | 南昌大学 | 4-硝基三苯胺的合成方法 |
-
2007
- 2007-09-28 CN CN2007101395431A patent/CN101121668B/zh not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000239235A (ja) * | 1998-12-25 | 2000-09-05 | Hodogaya Chem Co Ltd | トリアリールアミン誘導体の製造方法 |
DE19963009A1 (de) * | 1999-12-22 | 2001-08-09 | Syntec Ges Fuer Chemie Und Tec | Verfahren zur Herstellung von Arylaminen |
DE10002561A1 (de) * | 2000-01-19 | 2001-07-26 | Syntec Ges Fuer Chemie Und Tec | Verfahren zur Herstellung von Arylaminen |
CN101012171A (zh) * | 2007-02-02 | 2007-08-08 | 南昌大学 | 4-硝基三苯胺的合成方法 |
Non-Patent Citations (2)
Title |
---|
李伟章等.微波辐射促进N-烷基化邻硝基苯胺的合成.有机化学.2002,22(7),511-514. * |
王金芳等.二苯胺和碘苯反应合成三苯胺.化学试剂.2004,26(1),35-36. * |
Also Published As
Publication number | Publication date |
---|---|
CN101121668A (zh) | 2008-02-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101121668B (zh) | 4,4’-二甲基三苯胺的合成方法 | |
CN107043359A (zh) | 一种丙硫菌唑中间体的制备方法 | |
CN104370724B (zh) | 一种芴酮衍生物及其制备方法,以及合成芴酮的氧化还原方法 | |
CN108689866B (zh) | 一种(r)-3-氨基丁醇的合成方法 | |
CN110078633B (zh) | 一种4-氟-3-甲氧基-5-甲基苯胺盐酸盐制备方法 | |
CN114438523B (zh) | 一种绿色高效的苯并噻吩类化合物电化学合成方法 | |
CN108047050B (zh) | 一种以卤代氘代甲烷合成氘代二甲胺盐的方法 | |
CN114957125A (zh) | 一种4-硝基5-硝胺吡唑的合成方法 | |
US10138187B2 (en) | Process for the synthesis of 9,9-bis(hydroxymethyl)fluorene | |
CN113105357A (zh) | 一种新型对芳基偶氮苯酚衍生物的合成方法及其应用 | |
EP2394980A1 (en) | Aromatic amino compound manufacturing method | |
Hafner et al. | Preparation of 2-Imino-and 2-Nitrimine-1, 3-diazacycloalkanes | |
CN101786956B (zh) | N-酰基化二苯胺或其环上取代的衍生物的脱酰基化方法 | |
RU2425031C1 (ru) | Способ получения 3-замещенных 2-амино-1-гидрокси-5,6-дицианоиндолов на основе 4-бром-5-нитрофталонитрила | |
EP3303277B1 (en) | Process for the synthesis of 9,9-bis(methoxymethyl)fluorene | |
CA2510270C (en) | Process for producing anthracene diether | |
US20190194104A1 (en) | Process for the synthesis of 9,9-bis(hydroxymethyl)fluorene | |
CN100548967C (zh) | 4,4’,4”-三硝基三苯胺的合成方法 | |
CN112358437B (zh) | 一步合成4,4’-双(9h-咔唑-9-基)联苯类化合物的方法 | |
CN115746021B (zh) | 一种7-氨基-6-硝基苯并二氧化呋咱及其异构体的合成方法 | |
CN101314593B (zh) | 一种合成苯并咪唑啉衍生物的方法 | |
CN108912052B (zh) | 一种氰霜唑的制备方法 | |
CN103288737B (zh) | 一种亚氨基芪的合成方法 | |
CN102070427B (zh) | 一种氟鼠酮及其中间体的合成方法 | |
CN102633708B (zh) | 一种中间体9-(2-羟乙基)咔唑的合成与纯化方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C53 | Correction of patent for invention or patent application | ||
CB03 | Change of inventor or designer information |
Inventor after: Cui Jianlan Inventor after: Wang Baoguo Inventor after: Wang Limin Inventor after: Chen Yafang Inventor before: Cui Jianlan Inventor before: Cao Duanlin Inventor before: Wang Limin Inventor before: Cai Jianbo |
|
COR | Change of bibliographic data |
Free format text: CORRECT: INVENTOR; FROM: CUI JIANLAN CAO DUANLIN WANG LIMIN CAI JIANBO TO: CUI JIANLAN WANG BAOGUO WANG LIMIN CHEN YAFANG |
|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C17 | Cessation of patent right | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20110119 Termination date: 20120928 |