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2-Methyl-4-nitrophenol → Dimethyl{2-[(2-methyl-4-nitrophenyl)oxy]ethyl}amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Methyl-4-nitrophenol | HCID 7442 | — |
| 反応物 | 2-Chloro-N,N-dimethylethylamine | HCID 7901 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | Dimethyl{2-[(2-methyl-4-nitrophenyl)oxy]ethyl}amine | HCID 58377223 | 20.5% |
反応手順
Acetonitrile (30 mL) solution of 2 g of 2-methyl-4-nitrophenol, 1.87 g of 2-dimethylaminoethyl chloride and 5.4 g of potassium carbonate was stirred at 120° C. for 23 hours. The reaction liquid was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate. The organic layer was washed with water, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the crude product was purified through silica gel column chromatography (chloroform/methanol) to obtain 600 mg of the entitled compound as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07935708B2 |
| 出典データセット | uspto-grants-2011_05 |
| ORD ID | ord-bd50beb18dbb4ea389c1ea8587e0103b |
| 出典メモ | uspto-grants-2011_05 |