関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 5-Methoxy-2,4-dinitrophenol | HCID 266795 | — |
| 反応物 | N,N-dimethylformamide;hydrochloride | HCID 10920465 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4,6-Dinitroresorcinol | HCID 61158 | 95% |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05463129 |
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| 出典データセット | uspto-grants-1995_10 |
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| ORD ID | ord-764ba658150c4f60b7e970e197d8ecff |
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| 出典メモ | uspto-grants-1995_10 |
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