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Lithium Hydroxide → 2-(4-Methylsulfanyl-phenoxy)-nicotinic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Lithium Hydroxide | HCID 3939 | — |
| 反応物 | 2-(4-Methylsulfanyl-phenoxy)-nicotinic acid methyl ester | HCID 58746179 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-(4-Methylsulfanyl-phenoxy)-nicotinic acid | HCID 21877137 | 94.7% |
反応手順
2-(4-methylsulfanyl-phenoxy)-nicotinic acid methyl ester (10.36 g, 37.6 mmol) was dissolved in tetrahydrofuran (140 ml) and 1M aqueous lithium hydroxide solution (94 ml, 94 mmol) was added. The reaction was stirred at room temperature for 18 h and the tetrahydrofuran was removed under reduced pressure. The residue was acidified to pH1 with concentrated hydrochloric acid and the resulting precipitate was filtered, washed with water (2×10 ml), diethyether (3×10 ml) and dried in vacuo to give 2-(4-methylsulfanyl-phenoxy)-nicotinic acid (9.3 g) as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07141586B2 |
| 出典データセット | uspto-grants-2006_11 |
| ORD ID | ord-b6cd68847df546618176856ee718bfc1 |
| 出典メモ | uspto-grants-2006_11 |