HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740884Generated: November 1, 2026
5-Chloro-2-nitroaniline → HCID 21834282, compound
https://huagongshe.com/reaction/1740884
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Chloro-2-nitroaniline | HCID 74218 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178418642 | HCID 178418642 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21834282 | HCID 21834282 | — |
Reaction Steps
A 2-liter round-bottomed flask is charged with 35.2 g (0.369 mol) of 4-hydroxypyridine and 250 ml of anhydrous dimethylformamide (DMF). Under nitrogen, 42 g (0.369 mol) of potassium tert-butylate are added portionwise while the temperature is maintained at 15-20° C. with a water/ice bath. After the addition, the mixture is stirred for 2 hours and a pale yellow solution is obtained. 60 g (0.358 mol) of 2-nitro-5-chloroaniline are then added and an intense red coloration is obtained. The mixture is brought to 100° C. for 6 hours and then allowed to cool overnight. The DMF is evaporated off and water is then added; a precipitate is obtained, which is filtered off and washed with isopropanol in the heated state and then dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05972968 |
|---|
| Source dataset | uspto-grants-1999_10 |
|---|
| ORD ID | ord-4fbe12e40aaa44d48d934f699e4585e0 |
|---|
| Source note | uspto-grants-1999_10 |
|---|