HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868524Generated: October 30, 2026
N,N-Dimethylaniline → HCID 14280609, compound
https://huagongshe.com/reaction/868524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178517133 | HCID 178517133 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 14280609 | HCID 14280609 | — |
Reaction Steps
To a suspension of 1-(trifluoromethyl)[1,2,4]triazolo[4,3-a]quinoxalin-4-ol (2.5 g; 0.01 mole) in 60 ml of acetonitrile, Et4N+Cl- (2.4 g) followed by N,N-dimethylaniline (1.7 ml) and POCl3 (3.75 ml) were added. Reaction mixture was refluxed for 20 hours. Volatiles were removed under reduced pressure, residue was dissolved in CHCl3 (100 ml) and added to the ice-water. Layers were separated, the aqueous layer was extracted with chloroform (2×200 ml). The combined extract was washed with 5% NaHCO3 (2×120 ml) followed by brine (2×50 ml). It was dried over MgSO4, filtered, and volatiles were removed. The residue was crystallized from chloroform-hexane affording 1.78 g of 4-chloro-1-(trifluoromethyl)[1,2,4]triazolo[4,3-a]quinoxaline; mass spectrum m/e, 272 (m+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04780464 |
|---|
| Source dataset | uspto-grants-1988_10 |
|---|
| ORD ID | ord-ec926e74861146a3bed16f7805ee13e0 |
|---|
| Source note | uspto-grants-1988_10 |
|---|