HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-Cyano-2-hydroxy-1-(4-trifluoromethylphenyl)aminothiocarbonylpropene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 5-Methyl-4-(4-trifluoromethylphenyl)aminothiocarbonylisoxazole | HCID 15858807 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Cyano-2-hydroxy-1-(4-trifluoromethylphenyl)aminothiocarbonylpropene | HCID 136395989 | 71.4% |
Reaction Steps
A solution of 7.0 grams of 5-methyl-4-(4-trifluoromethylphenyl)aminothiocarbonylisoxazole and 5 ml of 1,8-diazabicyclo[5.4.0]undec-7-ene in 50 ml of ethanol was heated at 80° C. for 8 hours. The reaction mixture was cooled to room temperature and acidified with 6N hydrochloric acid solution until pH 2. The mixture was then cooled in an ice-water bath for 30 minutes and the solid was filtered, washed with a chilled solution of ethanol and water (2:1) and dried by suction to provide 5.0 grams of 1-cyano-2-hydroxy-1-(4-trifluoromethylphenyl)aminothiocarbonylpropene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05721277 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-bebb45e9bd424269a8c9da4e0bbffa92 |
| Source note | uspto-grants-1998_02 |