CN1098899C - 蒽并吡啶酮类染料中间体及其生产方法 - Google Patents
蒽并吡啶酮类染料中间体及其生产方法 Download PDFInfo
- Publication number
- CN1098899C CN1098899C CN99114563A CN99114563A CN1098899C CN 1098899 C CN1098899 C CN 1098899C CN 99114563 A CN99114563 A CN 99114563A CN 99114563 A CN99114563 A CN 99114563A CN 1098899 C CN1098899 C CN 1098899C
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- CN
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- Prior art keywords
- bromination
- temperature
- acidylate
- haloalkane
- closed loop
- 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.)
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- XBNVWXKPFORCRI-UHFFFAOYSA-N 2h-naphtho[2,3-f]quinolin-1-one Chemical compound C1=CC=CC2=CC3=C4C(=O)CC=NC4=CC=C3C=C21 XBNVWXKPFORCRI-UHFFFAOYSA-N 0.000 title claims abstract description 7
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 238000005893 bromination reaction Methods 0.000 claims abstract description 29
- 230000031709 bromination Effects 0.000 claims abstract description 25
- 238000005917 acylation reaction Methods 0.000 claims abstract description 10
- 230000010933 acylation Effects 0.000 claims abstract description 7
- SVTDYSXXLJYUTM-UHFFFAOYSA-N disperse red 9 Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC SVTDYSXXLJYUTM-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000007670 refining Methods 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 3
- 239000000463 material Substances 0.000 claims description 17
- 239000000975 dye Substances 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 14
- 238000009413 insulation Methods 0.000 claims description 10
- 238000005516 engineering process Methods 0.000 claims description 9
- 150000001350 alkyl halides Chemical class 0.000 claims description 8
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims description 6
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 5
- HGUMYMRHRBCLIU-UHFFFAOYSA-N N1=CC=CC2=C(C=C3C(CC(C=C3)=O)=C3)C3=CC=C21 Chemical compound N1=CC=CC2=C(C=C3C(CC(C=C3)=O)=C3)C3=CC=C21 HGUMYMRHRBCLIU-UHFFFAOYSA-N 0.000 claims description 4
- 239000013078 crystal Substances 0.000 claims description 4
- 238000001914 filtration Methods 0.000 claims description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 4
- 238000007363 ring formation reaction Methods 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 3
- 238000004821 distillation Methods 0.000 claims description 3
- 230000003472 neutralizing effect Effects 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 238000002425 crystallisation Methods 0.000 claims description 2
- 230000008025 crystallization Effects 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 238000006386 neutralization reaction Methods 0.000 claims description 2
- 239000002994 raw material Substances 0.000 claims description 2
- 238000002791 soaking Methods 0.000 claims description 2
- NFWKNMBLIMXKDM-UHFFFAOYSA-N n-methylanthracen-1-amine Chemical compound C1=CC=C2C=C3C(NC)=CC=CC3=CC2=C1 NFWKNMBLIMXKDM-UHFFFAOYSA-N 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims 1
- TVPQEXARYLILTB-UHFFFAOYSA-N 12-bromo-14-methyl-14-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2,4,6,9(17),10,12-heptaene-8,15-dione Chemical compound O=C1C2=CC=CC=C2C2=CC(=O)N(C)C3=C(Br)C=CC1=C32 TVPQEXARYLILTB-UHFFFAOYSA-N 0.000 abstract 1
- 238000013508 migration Methods 0.000 description 4
- 230000005012 migration Effects 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (3)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN99114563A CN1098899C (zh) | 1999-11-22 | 1999-11-22 | 蒽并吡啶酮类染料中间体及其生产方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN99114563A CN1098899C (zh) | 1999-11-22 | 1999-11-22 | 蒽并吡啶酮类染料中间体及其生产方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1296999A CN1296999A (zh) | 2001-05-30 |
CN1098899C true CN1098899C (zh) | 2003-01-15 |
Family
ID=5277630
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CN99114563A Expired - Fee Related CN1098899C (zh) | 1999-11-22 | 1999-11-22 | 蒽并吡啶酮类染料中间体及其生产方法 |
Country Status (1)
Country | Link |
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CN (1) | CN1098899C (zh) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104725315A (zh) * | 2013-12-21 | 2015-06-24 | 江苏道博化工有限公司 | 一种制备溶剂红149的方法 |
CN106749019B (zh) * | 2016-11-29 | 2019-10-25 | 安徽清科瑞洁新材料有限公司 | 一种溶剂红52染料的环保制备方法 |
CN106674111A (zh) * | 2016-12-08 | 2017-05-17 | 江苏道博化工有限公司 | 一种合成4‑溴‑n‑甲基‑1(n)‑9‑蒽并吡啶酮的方法 |
CN108586338A (zh) * | 2018-05-10 | 2018-09-28 | 安徽清科瑞洁新材料有限公司 | 一种溶剂红149染料的低污染生产方法 |
CN108587228A (zh) * | 2018-05-10 | 2018-09-28 | 安徽清科瑞洁新材料有限公司 | 一种溶剂红149染料的生产方法 |
CN108587227A (zh) * | 2018-05-10 | 2018-09-28 | 安徽清科瑞洁新材料有限公司 | 一种高得率溶剂红149染料的生产方法 |
CN111138305A (zh) * | 2019-12-20 | 2020-05-12 | 南京金浩医药科技有限公司 | 一种1-甲氨基-4-溴蒽醌的制备方法 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1230203A (zh) * | 1996-09-11 | 1999-09-29 | 日本化药株式会社 | 蒽并吡啶酮化合物、水基油墨组合物和着色制品 |
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1999
- 1999-11-22 CN CN99114563A patent/CN1098899C/zh not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1230203A (zh) * | 1996-09-11 | 1999-09-29 | 日本化药株式会社 | 蒽并吡啶酮化合物、水基油墨组合物和着色制品 |
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CN1296999A (zh) | 2001-05-30 |
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C06 | Publication | ||
PB01 | Publication | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C56 | Change in the name or address of the patentee |
Owner name: YABANG INVESTMENT HOLDING GROUP CO., LTD. Free format text: FORMER NAME: YABANG GROUP CO, JIANGSU |
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CP03 | Change of name, title or address |
Address after: 213163 Changzhou Province, Wujin City, the town of cattle, the people of the West Road, No. 105, No. Patentee after: Yabang Group Co., Ltd. Address before: 213163 Niu Tong Bridge, South Gate, Changzhou, Jiangsu Patentee before: Yabang Group Co, Jiangsu |
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EE01 | Entry into force of recordation of patent licensing contract |
Assignee: Anhui Yabang Chemical Co., Ltd. Assignor: Yabang Group Co., Ltd. Contract record no.: 2011340000350 Denomination of invention: Intermediate of anthracenopyridone dye and its preparing process Granted publication date: 20030115 License type: Exclusive License Open date: 20010530 Record date: 20110817 |
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CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20030115 Termination date: 20141122 |
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EXPY | Termination of patent right or utility model |