Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 5-Methoxy-2,4-dinitrophenol | HCID 266795 | — |
| Edukt | N,N-dimethylformamide;hydrochloride | HCID 10920465 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4,6-Dinitroresorcinol | HCID 61158 | 95% |
Reaktionsschritte
To a 100 mL round-bottom flask is added 2.14 g (10 mmol) of 5-methoxy-2,4-dinitrophenol (MDNP) and 1.31 g (12 mmol) of DMF-HCl in 30 mL of N,N-dimethylformamide (DMF). This mixture is stirred at 130° C. and monitored by High Pressure Liquid Chromatography (HPLC). After 8.5 hours essentially no MDNP is observed by HPLC. The reaction mixture is poured into 100 mL of 1N HCl, and extracted with ethyl acetate (EtOAc, 3×30 mL). The combined organics are washed with a single portion of 0.1N HCl, dried (Na2SO4) and concentrated by rotary evaporation to give crude 4,6-dinitroresorcinol (DNR) as a yellow solid (1.9 g, 95% yield): melting point (m.p.) 205° C. to 210° C., 1H NMR (CDCl3)δ11.03 (s,2H), 9.08 (s,1H), 6.82 (s,1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05463129 |
|---|
| Quelldatensatz | uspto-grants-1995_10 |
|---|
| ORD ID | ord-764ba658150c4f60b7e970e197d8ecff |
|---|
| Quellennotiz | uspto-grants-1995_10 |
|---|