CN1872402A - N-烷基邻苯二甲酰亚胺混合溶剂的制备方法 - Google Patents
N-烷基邻苯二甲酰亚胺混合溶剂的制备方法 Download PDFInfo
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- CN1872402A CN1872402A CN 200510026284 CN200510026284A CN1872402A CN 1872402 A CN1872402 A CN 1872402A CN 200510026284 CN200510026284 CN 200510026284 CN 200510026284 A CN200510026284 A CN 200510026284A CN 1872402 A CN1872402 A CN 1872402A
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- alkyl
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- 239000012046 mixed solvent Substances 0.000 title claims abstract description 24
- 238000000034 method Methods 0.000 title claims description 18
- 125000000217 alkyl group Chemical group 0.000 title claims description 6
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims abstract description 28
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000000203 mixture Substances 0.000 claims description 32
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 26
- 238000010992 reflux Methods 0.000 claims description 21
- 238000002360 preparation method Methods 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 16
- 150000003141 primary amines Chemical class 0.000 claims description 16
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 12
- 150000001412 amines Chemical class 0.000 claims description 10
- -1 alkyl phthalic imide Chemical compound 0.000 claims description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 5
- 150000004996 alkyl benzenes Chemical class 0.000 claims description 4
- CYMRPDYINXWJFU-UHFFFAOYSA-N 2-carbamoylbenzoic acid Chemical compound NC(=O)C1=CC=CC=C1C(O)=O CYMRPDYINXWJFU-UHFFFAOYSA-N 0.000 claims description 2
- 238000009833 condensation Methods 0.000 claims description 2
- 230000005494 condensation Effects 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims description 2
- 239000007810 chemical reaction solvent Substances 0.000 abstract description 3
- 238000006482 condensation reaction Methods 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 239000008096 xylene Substances 0.000 description 15
- 239000000376 reactant Substances 0.000 description 14
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 13
- 238000010792 warming Methods 0.000 description 11
- 150000003738 xylenes Chemical class 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000004821 distillation Methods 0.000 description 9
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 9
- 238000005292 vacuum distillation Methods 0.000 description 9
- DLKDEVCJRCPTLN-UHFFFAOYSA-N 2-butylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCC)C(=O)C2=C1 DLKDEVCJRCPTLN-UHFFFAOYSA-N 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 8
- 238000004128 high performance liquid chromatography Methods 0.000 description 7
- VPLDXHDOGVIETL-UHFFFAOYSA-N 2-propan-2-ylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(C(C)C)C(=O)C2=C1 VPLDXHDOGVIETL-UHFFFAOYSA-N 0.000 description 6
- 238000013019 agitation Methods 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 6
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 5
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 4
- HZFOJDJUDSUXSX-UHFFFAOYSA-N 2-(butylcarbamoyl)benzoic acid Chemical compound CCCCNC(=O)C1=CC=CC=C1C(O)=O HZFOJDJUDSUXSX-UHFFFAOYSA-N 0.000 description 4
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 4
- OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical compound CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- ZIKLMTDFHRNNRL-UHFFFAOYSA-N 2-(propan-2-ylcarbamoyl)benzoic acid Chemical compound CC(C)NC(=O)C1=CC=CC=C1C(O)=O ZIKLMTDFHRNNRL-UHFFFAOYSA-N 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 3
- NAYYNDKKHOIIOD-UHFFFAOYSA-N phthalamide Chemical compound NC(=O)C1=CC=CC=C1C(N)=O NAYYNDKKHOIIOD-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- YNELRWKTPWFDCW-UHFFFAOYSA-N 2-(butan-2-ylcarbamoyl)benzoic acid Chemical compound CCC(C)NC(=O)C1=CC=CC=C1C(O)=O YNELRWKTPWFDCW-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000006837 decompression Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000004811 liquid chromatography Methods 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 2
- 235000013599 spices Nutrition 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 150000000182 1,3,5-triazines Chemical class 0.000 description 1
- XDIAMRVROCPPBK-UHFFFAOYSA-N 2,2-dimethylpropan-1-amine Chemical compound CC(C)(C)CN XDIAMRVROCPPBK-UHFFFAOYSA-N 0.000 description 1
- VKMFCUYJBIEWLN-UHFFFAOYSA-N 2-(2,2-dimethylpropylcarbamoyl)benzoic acid Chemical compound CC(C)(C)CNC(=O)C1=CC=CC=C1C(O)=O VKMFCUYJBIEWLN-UHFFFAOYSA-N 0.000 description 1
- UKVAJXRECGGFJZ-UHFFFAOYSA-N 2-(ethylcarbamoyl)benzoic acid Chemical compound CCNC(=O)C1=CC=CC=C1C(O)=O UKVAJXRECGGFJZ-UHFFFAOYSA-N 0.000 description 1
- GPWMLCQYRAZVOI-UHFFFAOYSA-N 2-(pentan-2-ylcarbamoyl)benzoic acid Chemical compound CCCC(C)NC(=O)C1=CC=CC=C1C(O)=O GPWMLCQYRAZVOI-UHFFFAOYSA-N 0.000 description 1
- LXXQYKPFXHMUKE-UHFFFAOYSA-N 2-(pentylcarbamoyl)benzoic acid Chemical compound CCCCCNC(=O)C1=CC=CC=C1C(O)=O LXXQYKPFXHMUKE-UHFFFAOYSA-N 0.000 description 1
- RLARUBPTQYKZKA-UHFFFAOYSA-N 2-propylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCC)C(=O)C2=C1 RLARUBPTQYKZKA-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- 101800000021 N-terminal protease Proteins 0.000 description 1
- XNEFYCZVKIDDMS-UHFFFAOYSA-N avobenzone Chemical compound C1=CC(OC)=CC=C1C(=O)CC(=O)C1=CC=C(C(C)(C)C)C=C1 XNEFYCZVKIDDMS-UHFFFAOYSA-N 0.000 description 1
- 229960005193 avobenzone Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229940072395 n-butylphthalimide Drugs 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- 229960001173 oxybenzone Drugs 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical class CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
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- Indole Compounds (AREA)
Abstract
Description
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CNB2005100262842A CN100368066C (zh) | 2005-05-30 | 2005-05-30 | N-烷基邻苯二甲酰亚胺混合溶剂的制备方法 |
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CNB2005100262842A CN100368066C (zh) | 2005-05-30 | 2005-05-30 | N-烷基邻苯二甲酰亚胺混合溶剂的制备方法 |
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Publication Number | Publication Date |
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CN1872402A true CN1872402A (zh) | 2006-12-06 |
CN100368066C CN100368066C (zh) | 2008-02-13 |
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CNB2005100262842A Active CN100368066C (zh) | 2005-05-30 | 2005-05-30 | N-烷基邻苯二甲酰亚胺混合溶剂的制备方法 |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101498107B (zh) * | 2008-07-11 | 2012-04-25 | 杭州传化精细化工有限公司 | 一种修色剂及其制备方法 |
CN108383772A (zh) * | 2018-03-12 | 2018-08-10 | 江苏海云花新材料有限公司 | 一种n-烷基邻苯二甲酰亚胺制备方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5536846A (en) * | 1994-05-27 | 1996-07-16 | General Electric Company | Process for preparing bis(ether anhydrides) using alkylamine derived bisimides having low melting temperatures |
US6306373B1 (en) * | 2000-08-17 | 2001-10-23 | Phoenix Research Corporation | Mixed n-butyl and iso-propyl phthalamide compounds as sunscreen solubilizers |
US20040151677A1 (en) * | 2002-12-16 | 2004-08-05 | Societe L'oreal, S.A. | 1,3,5-Triazine sunscreens solubilized in mixed phthalimide eutectics |
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2005
- 2005-05-30 CN CNB2005100262842A patent/CN100368066C/zh active Active
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101498107B (zh) * | 2008-07-11 | 2012-04-25 | 杭州传化精细化工有限公司 | 一种修色剂及其制备方法 |
CN108383772A (zh) * | 2018-03-12 | 2018-08-10 | 江苏海云花新材料有限公司 | 一种n-烷基邻苯二甲酰亚胺制备方法 |
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Publication number | Publication date |
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CN100368066C (zh) | 2008-02-13 |
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