HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 6-chloroquinoxaline-2,3-dicarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-Chloro-1,2-diaminobenzene | HCID 7263 | — |
| Reactant | Diiminobutanedinitrile | HCID 119924 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-chloroquinoxaline-2,3-dicarbonitrile | HCID 303865 | 59.5% |
Reaction Steps
A mixture of 0.5 g (4.7 mmols) of the diiminosuccinonitrile and 0.67 g (4.7 mmols) of 4-chloro-1,2-phenylenediamine was slowly added to 10 ml of trifluoroacetic acid at about 20° C. over a period of 30 minutes, and the resulting mixture was stirred at room temperature for 8 hours and then allowed to stand overnight. To the reaction mixture was added 50 ml water, and the solid precipitated was filtered and sufficiently washed with water. The solid thus obtained was dried under reduced pressure, followed by a silica gel column chromatography (eluent: hexane/ethyl acetate=75/25) and then recrystallization from chloroform/ethanol, whereby 0.6 g (59%) of 6-chloro-2,3-dicyanoquinoxaline was obtained as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665875 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-0cb6c80ab55b44c3b9a90a2e23c200e5 |
| Source note | uspto-grants-1997_09 |