HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1160839Erstellt: 25. Oktober 2026
Methylamine → 2,6-Dimethyl-4-[3-(methylamino)-4-nitrophenoxy]aniline
https://huagongshe.com/reaction/1160839
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methylamine | HCID 6329 | — |
| Edukt | 2,4-Dichloronitrobenzene | HCID 11899 | — |
| Edukt | 4-Amino-3,5-dimethylphenol | HCID 76543 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 2,6-Dimethyl-4-[3-(methylamino)-4-nitrophenoxy]aniline | HCID 66701665 | 67% |
Reaktionsschritte
To a solution of 2,4-dichloronitrobenzene (3.0 g) in N,N-dimethylacetamide (30 ml) was added a 40% aqueous solution of methylamine (4.9 g) at room temperature, and the resulting mixture was stirred at 75-80° C. for 1.5 hours. To the reaction mixture were added 4-amino-3,5-dimethylphenol (2.2 g), potassium t-butoxide (3.5 g), and N,N-dimethylacetamide (15 ml), and the resulting mixture was stirred at the same temperature for 3 hours. After stirring, water (60 ml) was added to the reaction mixture, and the resulting mixture was cooled gradually to room temperature. The crystalline solid precipitated was collected by filtration and dried in vacuo to afford the title compound (3.0 g, yield: 67%) as a yellow crystalline solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07816552B2 |
|---|
| Quelldatensatz | uspto-grants-2010_10 |
|---|
| ORD ID | ord-553cb165e6454b8583fe610a05b79e66 |
|---|
| Quellennotiz | uspto-grants-2010_10 |
|---|