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Potassium Hydroxide → 6-Bromo-1-benzothiophene-2-carboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 6-Bromo-benzo[b]thiophene-2-carboxylic acid methyl ester | HCID 22474078 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 6-Bromo-1-benzothiophene-2-carboxylic acid | HCID 13567980 | — |
反応手順
A solution of 4.0 g (14.8 mmol) of methyl 6-bromo-1-benzothiophene-2-carboxylate in 40 ml of a 1:1 mixture of THF and 2 N potassium hydroxide solution is stirred at room temperature for 2 h. The solvent is removed in vacuo, and the residue is acidified with concentrated hydrochloric acid. The resulting precipitate is filtered off with suction, washed with water and dried in vacuo at 50° C. 3.55 g (93.5% of theory) of the desired product are obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09433614B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-195c3d7f9ab44d679c042dadfc5e6873 |
| 出典メモ | uspto-grants-2016_09 |