HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1,3-Dimethyl-5-[4-chloro-2-(2,6-dichlorophenoxy)phenylcarbamoyl]-2-thiobarbituric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1,3-Dimethyl-5-ethoxycarbonyl-2-thiobarbituric acid | HCID 14053347 | — |
| Reactant | 4-Chloro-2-(2,6-dichlorophenoxy)aniline | HCID 14053348 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-Dimethyl-5-[4-chloro-2-(2,6-dichlorophenoxy)phenylcarbamoyl]-2-thiobarbituric acid | HCID 14053349 | — |
Reaction Steps
2.5 g (10 mmol) of 1,3-dimethyl-5-ethoxycarbonyl-2-thiobarbituric acid, 2.9 g (10 mmol) of 4-chloro-2-(2,6-dichlorophenoxy)aniline, 40 ml of ethanol and 3 ml of dimethylformamide are mixed and then boiled under reflux with stirring for 6 hours. The reaction mixture is then cooled and the resultant crystalline precipitate is isolated by filtration. If necessary, the crystalline precipitate can be recrystallised from a mixture of dioxane and ethanol. Melting point 254°-257° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670441 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-3a5c48c155c54b1cb3cc92ad34110ef5 |
| Source note | uspto-grants-1987_06 |