CN106478635A - 一种有机电致发光材料吲哚咔唑化合物的绿色合成方法 - Google Patents
一种有机电致发光材料吲哚咔唑化合物的绿色合成方法 Download PDFInfo
- Publication number
- CN106478635A CN106478635A CN201610724181.1A CN201610724181A CN106478635A CN 106478635 A CN106478635 A CN 106478635A CN 201610724181 A CN201610724181 A CN 201610724181A CN 106478635 A CN106478635 A CN 106478635A
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- Prior art keywords
- reaction
- carbazole compound
- indole carbazole
- synthesis method
- organic material
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- -1 indole carbazole compound Chemical class 0.000 title claims abstract description 19
- 239000011368 organic material Substances 0.000 title claims abstract description 8
- 238000001308 synthesis method Methods 0.000 title claims abstract description 8
- 238000006243 chemical reaction Methods 0.000 claims abstract description 34
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000000463 material Substances 0.000 claims abstract description 9
- JOVOSQBPPZZESK-UHFFFAOYSA-N phenylhydrazine hydrochloride Chemical compound Cl.NNC1=CC=CC=C1 JOVOSQBPPZZESK-UHFFFAOYSA-N 0.000 claims abstract description 9
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000002904 solvent Substances 0.000 claims abstract description 8
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 230000000977 initiatory effect Effects 0.000 claims abstract description 5
- 238000009835 boiling Methods 0.000 claims abstract description 3
- 239000012046 mixed solvent Substances 0.000 claims abstract description 3
- OILAIQUEIWYQPH-UHFFFAOYSA-N cyclohexane-1,2-dione Chemical compound O=C1CCCCC1=O OILAIQUEIWYQPH-UHFFFAOYSA-N 0.000 claims description 7
- 238000011084 recovery Methods 0.000 claims description 4
- HJSLFCCWAKVHIW-UHFFFAOYSA-N cyclohexane-1,3-dione Chemical compound O=C1CCCC(=O)C1 HJSLFCCWAKVHIW-UHFFFAOYSA-N 0.000 claims description 2
- AJAZMOFONMJGNP-WMZOPIPTSA-N n-[(2s)-4-methyl-1-oxo-1-[[(2s)-3-oxo-4-(pyridin-2-ylsulfonylamino)butan-2-yl]amino]pentan-2-yl]-1-benzofuran-2-carboxamide Chemical compound O=C([C@H](C)NC(=O)[C@@H](NC(=O)C=1OC2=CC=CC=C2C=1)CC(C)C)CNS(=O)(=O)C1=CC=CC=N1 AJAZMOFONMJGNP-WMZOPIPTSA-N 0.000 claims 1
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 abstract description 22
- 239000002253 acid Substances 0.000 abstract description 12
- 238000000034 method Methods 0.000 abstract description 10
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract description 6
- 239000007788 liquid Substances 0.000 abstract description 6
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 abstract description 5
- 239000002699 waste material Substances 0.000 abstract description 5
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000003054 catalyst Substances 0.000 abstract description 3
- 239000012535 impurity Substances 0.000 abstract description 3
- 239000002994 raw material Substances 0.000 abstract description 3
- 239000002351 wastewater Substances 0.000 abstract description 3
- XKLPBDMZJSWRBL-UHFFFAOYSA-N 3-benzoylcyclohexane-1,2-dione Chemical compound C=1C=CC=CC=1C(=O)C1CCCC(=O)C1=O XKLPBDMZJSWRBL-UHFFFAOYSA-N 0.000 abstract description 2
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 abstract description 2
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 abstract description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 6
- QJTQKPNNQVLHHO-UHFFFAOYSA-N 9h-carbazole;1h-indole Chemical compound C1=CC=C2NC=CC2=C1.C1=CC=C2C3=CC=CC=C3NC2=C1 QJTQKPNNQVLHHO-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000005160 1H NMR spectroscopy Methods 0.000 description 3
- JQPFYXFVUKHERX-UHFFFAOYSA-N 2-hydroxy-2-cyclohexen-1-one Natural products OC1=CCCCC1=O JQPFYXFVUKHERX-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 3
- 238000007171 acid catalysis Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 229940038531 phenylhydrazine hydrochloride Drugs 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000010189 synthetic method Methods 0.000 description 3
- 0 C*(Nc1ccccc1)ClC Chemical compound C*(Nc1ccccc1)ClC 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000007363 ring formation reaction Methods 0.000 description 2
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 2
- UFLWECJWSGWVHB-UHFFFAOYSA-N 1H-carbazole Chemical compound C1=CC=C2C3=CC=CCC3=NC2=C1 UFLWECJWSGWVHB-UHFFFAOYSA-N 0.000 description 1
- PAHTUDYIDUXQLG-UHFFFAOYSA-N C=C(c1cc(cccc2)c2[nH]1)N Chemical compound C=C(c1cc(cccc2)c2[nH]1)N PAHTUDYIDUXQLG-UHFFFAOYSA-N 0.000 description 1
- 230000004568 DNA-binding Effects 0.000 description 1
- 238000006069 Suzuki reaction reaction Methods 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 230000003592 biomimetic effect Effects 0.000 description 1
- BCDSSSXUYLVMQY-UHFFFAOYSA-N bis(2,4,6-trimethylphenyl)boron Chemical group CC1=CC(C)=CC(C)=C1[B]C1=C(C)C=C(C)C=C1C BCDSSSXUYLVMQY-UHFFFAOYSA-N 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- DCZFGQYXRKMVFG-UHFFFAOYSA-N cyclohexane-1,4-dione Chemical compound O=C1CCC(=O)CC1 DCZFGQYXRKMVFG-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- HLVSZSQYBQCBQG-UHFFFAOYSA-N indolo[3,2-b]carbazole Chemical class C12=CC=CC=C2N=C2C1=CC1=NC3=CC=CC=C3C1=C2 HLVSZSQYBQCBQG-UHFFFAOYSA-N 0.000 description 1
- VVVPGLRKXQSQSZ-UHFFFAOYSA-N indolo[3,2-c]carbazole Chemical class C1=CC=CC2=NC3=C4C5=CC=CC=C5N=C4C=CC3=C21 VVVPGLRKXQSQSZ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000005622 photoelectricity Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 238000007039 two-step reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
Abstract
Description
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107474257A (zh) * | 2017-07-13 | 2017-12-15 | 兰州大学 | 一种吲哚并咔唑共价有机框架材料及其合成方法 |
CN113461692A (zh) * | 2021-05-31 | 2021-10-01 | 贵州大学 | 一种吲哚咔唑衍生物的合成方法及其长余辉材料的制备方法 |
CN113956258A (zh) * | 2021-10-25 | 2022-01-21 | 中钢集团南京新材料研究院有限公司 | 一种采用酸性离子液体的吲哚并[2,3-a]咔唑的制备方法 |
Citations (5)
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CN101235012A (zh) * | 2008-02-29 | 2008-08-06 | 复旦大学 | 6-甲氧基-1,2,3,9-四氢-4h-咔唑-4-酮的制备方法 |
CN102598344A (zh) * | 2009-10-23 | 2012-07-18 | 新日铁化学株式会社 | 有机场致发光元件 |
CN103130824A (zh) * | 2011-11-24 | 2013-06-05 | 河南师范大学 | 一种高产率合成吲哚[3,2-b]咔唑的方法及其在有机太阳能电池中的应用 |
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WO2016112762A1 (zh) * | 2015-01-13 | 2016-07-21 | 广州华睿光电材料有限公司 | 化合物、包含其的混合物、组合物和有机电子器件 |
-
2016
- 2016-08-25 CN CN201610724181.1A patent/CN106478635B/zh active Active
Patent Citations (5)
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CN101235012A (zh) * | 2008-02-29 | 2008-08-06 | 复旦大学 | 6-甲氧基-1,2,3,9-四氢-4h-咔唑-4-酮的制备方法 |
CN102598344A (zh) * | 2009-10-23 | 2012-07-18 | 新日铁化学株式会社 | 有机场致发光元件 |
CN103130824A (zh) * | 2011-11-24 | 2013-06-05 | 河南师范大学 | 一种高产率合成吲哚[3,2-b]咔唑的方法及其在有机太阳能电池中的应用 |
KR20160041019A (ko) * | 2014-10-06 | 2016-04-15 | 희성소재 (주) | 헤테로고리 화합물 및 이를 이용한 유기 발광 소자 |
WO2016112762A1 (zh) * | 2015-01-13 | 2016-07-21 | 广州华睿光电材料有限公司 | 化合物、包含其的混合物、组合物和有机电子器件 |
Non-Patent Citations (2)
Title |
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何敬文: "《药物合成反应》", 31 December 1995 * |
秦瑞平,等: "一种改进的双费歇尔关环法合成吲哚[3,2-b]咔唑", 《科学通报》 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107474257A (zh) * | 2017-07-13 | 2017-12-15 | 兰州大学 | 一种吲哚并咔唑共价有机框架材料及其合成方法 |
CN107474257B (zh) * | 2017-07-13 | 2020-10-02 | 兰州大学 | 一种吲哚并咔唑共价有机框架材料及其合成方法 |
CN113461692A (zh) * | 2021-05-31 | 2021-10-01 | 贵州大学 | 一种吲哚咔唑衍生物的合成方法及其长余辉材料的制备方法 |
CN113956258A (zh) * | 2021-10-25 | 2022-01-21 | 中钢集团南京新材料研究院有限公司 | 一种采用酸性离子液体的吲哚并[2,3-a]咔唑的制备方法 |
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