HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266906Generated: October 31, 2026
4-Nitroaniline → HCID 178526680, compound
https://huagongshe.com/reaction/266906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitroaniline | HCID 7475 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4,5,6-Trichloro-1,2,3-triazine | HCID 12493611 | — |
| Reactant | HCID 21988082 | HCID 21988082 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178526680 | HCID 178526680 | 80.9% |
Reaction Steps
Para-nitroaniline (13.8 g) was dissolved into acetone (150 ml) at room temperature. 2,4,6-Trichlorotriazine (18.4 g) was dissolved into acetone (100 ml). Then the trichlorotriazine solution was dropwisely added to the p-nitroaniline solution as the p-nitroaniline solution was cooled with iced water. After the reaction was carried out for 2 hours at 0° C., an aqueous sodium bicarbonate solution (8.4 g of sodium bicarbonate being dissolved in 100 ml of water) was dropwisely added to the solution over 30 minutes. Then, the cooling was stopped by removing the ice bath and the solution was stirred until the temperature of the solution became room temperature. The reaction product was filtered off, washed with water and vacuum dried to obtain 23 g of 2,4-dichloro-6-p-nitroanilinotriazine. The chemical structure of the reaction product was confirmed by NMR and the melting point.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05652327 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-c5ffaf95e79648d2b17e8197db5f8b98 |
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| Source note | uspto-grants-1997_07 |
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