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Benzyl Bromide → 4-(Benzyloxy)-2-chloro-1-nitrobenzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl Bromide | HCID 7498 | — |
| 反応物 | 3-Chloro-4-nitrophenol | HCID 10283 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 4-(Benzyloxy)-2-chloro-1-nitrobenzene | HCID 819861 | — |
反応手順
A mixture of 3-chloro-4-nitrophenol (10 g, 0.058 mole), benzyl bromide (11.8 g, 0.069 mole), and potassium carbonate (16 g, 0.116 mole) in acetone is stirred, heated at reflux temperature for 17 hours, cooled and filtered. The filtrate is concentrated in vacuo to give a solid residue which is recrystallized from absolute ethanol to give the title compound, mp 82°-84.5° C., identified by elemental and NMR analyses.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05324711 |
| 出典データセット | uspto-grants-1994_06 |
| ORD ID | ord-f89a0f77bb17487ca27e8667cc139775 |
| 出典メモ | uspto-grants-1994_06 |