HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropyl Ether → 4-(4-Chloro-3-dimethylsulfamoylphenyl)-3-methyl-2-(2,4-dimethylphenyl-imino)-4-thiazoline hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-(2,4-Dimethylphenyl)-3-methylthiourea | HCID 3034214 | — |
| Reactant | 2-Bromo-4'-chloro-3'-dimethylsulfamoylacetophenone | HCID 20476846 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-(4-Chloro-3-dimethylsulfamoylphenyl)-3-methyl-2-(2,4-dimethylphenyl-imino)-4-thiazoline hydrobromide | HCID 20527233 | — |
Reaction Steps
3.41 g (0.01 mole) of 2-bromo-4'-chloro-3'-dimethylsulfamoyl-acetophenone are added to a solution of 1.83 g (0.01 mole) of 3-methyl-1-(2,4-dimethylphenyl)thiourea in 60 ml of glacial acetic acid and the mixture is stirred at room temperature for 20 minutes. It is then boiled for 20 minutes under a reflux condenser and allowed to cool, 60 ml of ethyl acetate or diisopropyl ether are added to the reaction mixture and the crystals are filtered off. Melting point 260°-264° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04346088 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-ca1870352c5b4abfafa75b730fe52dfd |
| Source note | uspto-grants-1982_08 |