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Potassium Hydroxide → 2-Nitro-5-(3-thienylmethoxy)phenol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 2-Fluoro-4-(3-thienylmethoxy)nitrobenzene | HCID 22010146 | — |
| 溶媒 | tert-Butanol | HCID 6386 | — |
| 生成物 | 2-Nitro-5-(3-thienylmethoxy)phenol | HCID 22010342 | — |
反応手順
A mixture of 2-fluoro-4-(3-thienylmethoxy)nitrobenzene (4.21 g), aqueous potassium hydroxide solution (50 mL; 50% w/v) and t-butanol (20 mL) is heated at reflux for 4 hours. It is then evaporated to dryness and the residue is partitioned between ethyl acetate (100 mL) and hydrochloric acid (100 mL; 1 N). The organic phase is washed with water (3×100 mL), dried over magnesium sulphate, filtered and evaporated, to give 2-nitro-5-(3-thienylmethoxy)phenol, in the form of a yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06211234B1 |
| 出典データセット | uspto-grants-2001_04 |
| ORD ID | ord-90c13fef15b74e0bbc01c05a818beff2 |
| 出典メモ | uspto-grants-2001_04 |