GB984811A - Process for the production of isothiazole and substituted isothiazole compounds - Google Patents
Process for the production of isothiazole and substituted isothiazole compoundsInfo
- Publication number
- GB984811A GB984811A GB3876662A GB3876662A GB984811A GB 984811 A GB984811 A GB 984811A GB 3876662 A GB3876662 A GB 3876662A GB 3876662 A GB3876662 A GB 3876662A GB 984811 A GB984811 A GB 984811A
- Authority
- GB
- United Kingdom
- Prior art keywords
- isothiazole
- methyl
- phenyl
- propylene
- ammonia
- 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
Links
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical compound C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 title abstract 4
- 150000003854 isothiazoles Chemical class 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 6
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 4
- 229910021529 ammonia Inorganic materials 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 3
- 235000010269 sulphur dioxide Nutrition 0.000 abstract 3
- 239000004291 sulphur dioxide Substances 0.000 abstract 3
- YUTQRQJTFPEEPB-UHFFFAOYSA-N 4-methyl-1,2-thiazole Chemical compound CC=1C=NSC=1 YUTQRQJTFPEEPB-UHFFFAOYSA-N 0.000 abstract 2
- GCJTZGLHWFXNSS-UHFFFAOYSA-N 5-phenyl-1,2-thiazole Chemical class S1N=CC=C1C1=CC=CC=C1 GCJTZGLHWFXNSS-UHFFFAOYSA-N 0.000 abstract 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 abstract 2
- SJNALLRHIVGIBI-UHFFFAOYSA-N allyl cyanide Chemical compound C=CCC#N SJNALLRHIVGIBI-UHFFFAOYSA-N 0.000 abstract 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N isopropyl alcohol Natural products CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 2
- -1 propylene isopropyl alcohol Chemical compound 0.000 abstract 2
- RKKGUHKROGFETL-UHFFFAOYSA-N 1,2-thiazole-3-carbonitrile Chemical compound N#CC=1C=CSN=1 RKKGUHKROGFETL-UHFFFAOYSA-N 0.000 abstract 1
- OCYPFRDEUKBLNI-UHFFFAOYSA-N 1,2-thiazole-4-carbonitrile Chemical compound N#CC=1C=NSC=1 OCYPFRDEUKBLNI-UHFFFAOYSA-N 0.000 abstract 1
- PCXTYKGTWQCNJI-UHFFFAOYSA-N 1,2-thiazole-4-carboxylic acid Chemical compound OC(=O)C=1C=NSC=1 PCXTYKGTWQCNJI-UHFFFAOYSA-N 0.000 abstract 1
- WOTIUKDGJBXFLG-UHFFFAOYSA-N 3-methyl-1,2-thiazole Chemical compound CC=1C=CSN=1 WOTIUKDGJBXFLG-UHFFFAOYSA-N 0.000 abstract 1
- RAUUYMXHIUAZCW-UHFFFAOYSA-N 4-phenyl-1,2-thiazole Chemical compound C1=NSC=C1C1=CC=CC=C1 RAUUYMXHIUAZCW-UHFFFAOYSA-N 0.000 abstract 1
- LBBKWEDRPDGXPM-UHFFFAOYSA-N 5-methyl-1,2-thiazole Chemical compound CC1=CC=NS1 LBBKWEDRPDGXPM-UHFFFAOYSA-N 0.000 abstract 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 abstract 1
- 101100097467 Arabidopsis thaliana SYD gene Proteins 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- 101100495925 Schizosaccharomyces pombe (strain 972 / ATCC 24843) chr3 gene Proteins 0.000 abstract 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- BVCZEBOGSOYJJT-UHFFFAOYSA-N ammonium carbamate Chemical compound [NH4+].NC([O-])=O BVCZEBOGSOYJJT-UHFFFAOYSA-N 0.000 abstract 1
- 235000012501 ammonium carbonate Nutrition 0.000 abstract 1
- 239000001099 ammonium carbonate Substances 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 abstract 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000005336 cracking Methods 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical group CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 abstract 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEZ9032A DE1168433B (de) | 1961-10-26 | 1961-10-26 | Verfahren zur Herstellung von Isothiazolen |
| DEZ0009388 | 1962-05-04 | ||
| DEZ9391A DE1193051B (de) | 1962-05-04 | 1962-05-04 | Verfahren zur Herstellung von Isothiazolen |
| DEZ9389A DE1198826B (de) | 1962-05-04 | 1962-05-04 | Verfahren zur Herstellung von Isothiazolen |
| DEZ9390A DE1183088B (de) | 1962-05-04 | 1962-05-04 | Verfahren zur Herstellung von Isothiazolen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB984811A true GB984811A (en) | 1965-03-03 |
Family
ID=27512349
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3876662A Expired GB984811A (en) | 1961-10-26 | 1962-10-12 | Process for the production of isothiazole and substituted isothiazole compounds |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE623633A (en(2012)) |
| CH (1) | CH416634A (en(2012)) |
| GB (1) | GB984811A (en(2012)) |
| SE (1) | SE308722B (en(2012)) |
-
0
- BE BE623633D patent/BE623633A/xx unknown
-
1962
- 1962-10-10 CH CH1188462A patent/CH416634A/de unknown
- 1962-10-12 GB GB3876662A patent/GB984811A/en not_active Expired
- 1962-10-26 SE SE1153162A patent/SE308722B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CH416634A (de) | 1966-07-15 |
| BE623633A (en(2012)) | |
| SE308722B (en(2012)) | 1969-02-24 |
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