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Ethyl Acetate → 4-(4-Benzyloxy-2-nitro-phenylsulfanyl)-phenylamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 4-Aminothiophenol | HCID 14510 | — |
| 反応物 | 5-Benzyloxy-2-chloro-nitrobenzene | HCID 11043622 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-(4-Benzyloxy-2-nitro-phenylsulfanyl)-phenylamine | HCID 66808306 | 83% |
反応手順
A solution of the compound prepared in Example 214A (1.0 g, 3.80 mmol), 4-aminothiophenol (0.5 g, 4.00 mmol), cesium carbonate (1.3 g, 4 mmol) in dimethylformamide (10 ml) was heated at 40° C. for 16 hours. Afterwards, ice water (50 mL) was added to the solution and the resultant slurry was treated with ethyl acetate (100 ml). The layers were separated and the organic layer was washed with 10% sodium bicarbonate and 10% sodium chloride, then dried over anhydrous sodium sulfate. The drying agent was filtered and solvent was removed under vacuum leaving an orange oil as the title compound, (1.1 g, 83%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07915411B2 |
| 出典データセット | uspto-grants-2011_03 |
| ORD ID | ord-ed2e7b96c85f4c33b00c948e44bd6bca |
| 出典メモ | uspto-grants-2011_03 |