HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291012Generated: October 31, 2026
Hydrochloric Acid → 2,4,5-Tris(4-aminophenyl)oxazole
https://huagongshe.com/reaction/2291012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,4,5-Tris(4-nitrophenyl)oxazole | HCID 13765876 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4,5-Tris(4-aminophenyl)oxazole | HCID 13750264 | — |
Reaction Steps
Then, 4.32 g (0.01 mol) of 2,4,5-tris(4-nitrophenyl)oxazole was mixed with 200 ml of N,N-dimethylformamide and 8 g of an iron powder (reduced iron available from Wako Pure Chemical Industries, Ltd.). To the resulting mixture, 4 ml of concentrated hydrochloric acid and 12 ml of water were added, and the mixture was heated to 100° C. while stirring well. After reacting for 1 hour, the reacting solution was neutralized to pH: 8 with a saturated aqueous solution of sodium carbonate, and while maintained at 100° C., it was filtered in a heated state. The filtrate was poured into 1 l of iced water. The white precipitate formed of 2,4,5-tris(4-aminophenyl)oxazole was filtered off and dried. Yield: 3.27 g (96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04619881 |
|---|
| Source dataset | uspto-grants-1986_10 |
|---|
| ORD ID | ord-2032d3b4acb44142b85a50e617b0c98f |
|---|
| Source note | uspto-grants-1986_10 |
|---|