CS219294B2 - Method of making the 4-chlor-5-amino-2-phenyl-3/2h/-pyridazine z 4,5-dichlor-2-phenyl-3/2h/-pyridazinone and ammonium - Google Patents
Method of making the 4-chlor-5-amino-2-phenyl-3/2h/-pyridazine z 4,5-dichlor-2-phenyl-3/2h/-pyridazinone and ammonium Download PDFInfo
- Publication number
- CS219294B2 CS219294B2 CS807318A CS731880A CS219294B2 CS 219294 B2 CS219294 B2 CS 219294B2 CS 807318 A CS807318 A CS 807318A CS 731880 A CS731880 A CS 731880A CS 219294 B2 CS219294 B2 CS 219294B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- phenyl
- pyridazinone
- amino
- naphthol
- chloro
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 title 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims abstract description 34
- WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 claims abstract description 24
- VKWCOHVAHQOJGU-UHFFFAOYSA-N 4,5-dichloro-2-phenylpyridazin-3-one Chemical compound O=C1C(Cl)=C(Cl)C=NN1C1=CC=CC=C1 VKWCOHVAHQOJGU-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000000034 method Methods 0.000 claims abstract description 16
- 239000003054 catalyst Substances 0.000 claims abstract description 15
- 229910021529 ammonia Inorganic materials 0.000 claims abstract description 14
- 238000006243 chemical reaction Methods 0.000 claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000012429 reaction media Substances 0.000 claims abstract description 8
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims abstract description 6
- 238000001914 filtration Methods 0.000 claims abstract description 6
- 239000012452 mother liquor Substances 0.000 claims abstract description 6
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 5
- HAKJEHJYRKVCIU-UHFFFAOYSA-N 4-amino-5-chloro-2-phenylpyridazin-3-one Chemical compound O=C1C(N)=C(Cl)C=NN1C1=CC=CC=C1 HAKJEHJYRKVCIU-UHFFFAOYSA-N 0.000 claims abstract description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 12
- 239000007858 starting material Substances 0.000 claims description 9
- GRFNBEZIAWKNCO-UHFFFAOYSA-N 3-pyridinol Chemical compound OC1=CC=CN=C1 GRFNBEZIAWKNCO-UHFFFAOYSA-N 0.000 claims description 8
- XQXPVVBIMDBYFF-UHFFFAOYSA-N 4-hydroxyphenylacetic acid Chemical compound OC(=O)CC1=CC=C(O)C=C1 XQXPVVBIMDBYFF-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 8
- IJFXRHURBJZNAO-UHFFFAOYSA-N 3-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=CC(O)=C1 IJFXRHURBJZNAO-UHFFFAOYSA-N 0.000 claims description 6
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 claims description 6
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 6
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 5
- YLKCHWCYYNKADS-UHFFFAOYSA-N 5-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(O)=CC=CC2=C1S(O)(=O)=O YLKCHWCYYNKADS-UHFFFAOYSA-N 0.000 claims description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- IULJSGIJJZZUMF-UHFFFAOYSA-N 2-hydroxybenzenesulfonic acid Chemical compound OC1=CC=CC=C1S(O)(=O)=O IULJSGIJJZZUMF-UHFFFAOYSA-N 0.000 claims description 3
- HKWPUUYEGGDLJF-UHFFFAOYSA-N 4-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=CC=C2C(O)=CC(S(O)(=O)=O)=CC2=C1 HKWPUUYEGGDLJF-UHFFFAOYSA-N 0.000 claims description 3
- SCOSSUFXFMVRJQ-UHFFFAOYSA-N 6-hydroxynaphthalene-1-sulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC2=CC(O)=CC=C21 SCOSSUFXFMVRJQ-UHFFFAOYSA-N 0.000 claims description 3
- MVEOHWRUBFWKJY-UHFFFAOYSA-N 7-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=CC(S(O)(=O)=O)=CC2=CC(O)=CC=C21 MVEOHWRUBFWKJY-UHFFFAOYSA-N 0.000 claims description 3
- GGOZGYRTNQBSSA-UHFFFAOYSA-N pyridine-2,3-diol Chemical compound OC1=CC=CN=C1O GGOZGYRTNQBSSA-UHFFFAOYSA-N 0.000 claims description 3
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 3
- 229960001755 resorcinol Drugs 0.000 claims description 3
- IAAKNVCARVEIFS-UHFFFAOYSA-M sodium;4-hydroxynaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(O)=CC=C(S([O-])(=O)=O)C2=C1 IAAKNVCARVEIFS-UHFFFAOYSA-M 0.000 claims description 3
- DOBIZWYVJFIYOV-UHFFFAOYSA-N 7-hydroxynaphthalene-1,3-disulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C(S(O)(=O)=O)C2=CC(O)=CC=C21 DOBIZWYVJFIYOV-UHFFFAOYSA-N 0.000 claims description 2
- HUYJTJXLNBOVFO-UHFFFAOYSA-N 7-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(O)=CC=C21 HUYJTJXLNBOVFO-UHFFFAOYSA-N 0.000 claims description 2
- 239000012467 final product Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 7
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 230000001172 regenerating effect Effects 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical compound OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 description 2
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
- 235000021536 Sugar beet Nutrition 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- VJWXIRQLLGYIDI-UHFFFAOYSA-N 4,5-dichloro-1h-pyridazin-6-one Chemical class OC1=NN=CC(Cl)=C1Cl VJWXIRQLLGYIDI-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- -1 compound compound Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000005580 one pot reaction Methods 0.000 description 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- 229940067157 phenylhydrazine Drugs 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D237/22—Nitrogen and oxygen atoms
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DK461379 | 1979-10-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS219294B2 true CS219294B2 (en) | 1983-03-25 |
Family
ID=8135124
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS807318A CS219294B2 (en) | 1979-10-31 | 1980-10-29 | Method of making the 4-chlor-5-amino-2-phenyl-3/2h/-pyridazine z 4,5-dichlor-2-phenyl-3/2h/-pyridazinone and ammonium |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4454318A (en]) |
| EP (1) | EP0028359B1 (en]) |
| JP (1) | JPS56501486A (en]) |
| AT (1) | ATE7026T1 (en]) |
| CS (1) | CS219294B2 (en]) |
| DD (1) | DD154016A5 (en]) |
| DE (1) | DE3067461D1 (en]) |
| DK (1) | DK150066C (en]) |
| FI (1) | FI63024C (en]) |
| IL (1) | IL61312A (en]) |
| RO (1) | RO81924A (en]) |
| UA (1) | UA7026A1 (en]) |
| WO (1) | WO1981001288A1 (en]) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3926905A1 (de) * | 1989-08-16 | 1991-02-21 | Basf Ag | Verfahren zur abtrennung und wiederverwertung von reststoffen aus dem abwasser der synthese von 5-amino-4-chlor-2-phenyl-3(2h)-pyridazinon |
| AU771700B2 (en) | 1999-03-31 | 2004-04-01 | Basf Aktiengesellschaft | Method for producing 4-amino-5-chloro-1-phenyl pyridazinone-(6) |
| JP2003231380A (ja) | 2002-02-12 | 2003-08-19 | Nhk Spring Co Ltd | 対象物の識別媒体及び識別方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL245646A (en]) * | 1960-03-19 | |||
| AT247355B (de) * | 1964-06-03 | 1966-06-10 | Basf Ag | Verfahren zur Herstellung von 1-Phenyl-4-amino-5-chlor-pyridazon-(6) |
| DE1620150A1 (de) * | 1965-03-19 | 1972-04-06 | Pavel Raposh | Verfahren zur Herstellung von Pyridazonen |
| FR1575643A (en]) * | 1968-03-28 | 1969-07-25 | ||
| DE2100685C2 (de) * | 1971-01-08 | 1983-09-22 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von reinen 4-Amino-5-halogen-pyridazonen-(6) |
| CS153812B1 (en]) * | 1971-01-15 | 1974-03-29 | ||
| CS158843B1 (en]) * | 1972-04-17 | 1974-12-27 | ||
| HU169505B (en]) * | 1974-05-22 | 1976-12-28 | ||
| DE2937421A1 (de) * | 1979-09-15 | 1981-04-09 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von 4-amino-5-chlor-1-phenylpyridazon-(6) |
-
1980
- 1980-10-17 JP JP50257780A patent/JPS56501486A/ja active Pending
- 1980-10-17 RO RO80103691A patent/RO81924A/ro unknown
- 1980-10-17 US US06/253,840 patent/US4454318A/en not_active Expired - Lifetime
- 1980-10-17 UA UA3304332A patent/UA7026A1/uk unknown
- 1980-10-17 WO PCT/DK1980/000062 patent/WO1981001288A1/en active IP Right Grant
- 1980-10-20 IL IL61312A patent/IL61312A/xx not_active IP Right Cessation
- 1980-10-22 DE DE8080106446T patent/DE3067461D1/de not_active Expired
- 1980-10-22 AT AT80106446T patent/ATE7026T1/de not_active IP Right Cessation
- 1980-10-22 EP EP80106446A patent/EP0028359B1/en not_active Expired
- 1980-10-29 CS CS807318A patent/CS219294B2/cs unknown
- 1980-10-31 DD DD80224876A patent/DD154016A5/de not_active IP Right Cessation
-
1981
- 1981-03-16 DK DK118081A patent/DK150066C/da not_active IP Right Cessation
- 1981-03-26 FI FI810936A patent/FI63024C/fi not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| UA7026A1 (uk) | 1995-03-31 |
| IL61312A (en) | 1984-11-30 |
| JPS56501486A (en]) | 1981-10-15 |
| IL61312A0 (en) | 1980-12-31 |
| EP0028359A1 (en) | 1981-05-13 |
| EP0028359B1 (en) | 1984-04-11 |
| FI810936L (fi) | 1981-05-01 |
| DE3067461D1 (en) | 1984-05-17 |
| DK150066B (da) | 1986-12-01 |
| ATE7026T1 (de) | 1984-04-15 |
| RO81924A (ro) | 1984-05-12 |
| DK150066C (da) | 1987-06-29 |
| DD154016A5 (de) | 1982-02-17 |
| DK118081A (da) | 1981-05-14 |
| US4454318A (en) | 1984-06-12 |
| WO1981001288A1 (en) | 1981-05-14 |
| FI63024C (fi) | 1983-04-11 |
| FI63024B (fi) | 1982-12-31 |
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