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Aluminium lithium hydride → [2-(2-Methyl-benzo[b]thiophen-3-ylsulfanyl)-phenyl]-methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 反応物 | 2-(2-Methyl-benzo[b]thiophen-3-ylsulfanyl)-benzoic acid methyl ester | HCID 68898083 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | [2-(2-Methyl-benzo[b]thiophen-3-ylsulfanyl)-phenyl]-methanol | HCID 68898143 | — |
反応手順
Lithium aluminum hydride (250 mg, 6.6 mmol) is added to a solution of 2-(2-methyl-benzo[b]thiophen-3-ylsulfanyl)-benzoic acid methyl ester (651 mg, 2.07 mmol) in 10 mL dry THF at 0° C. The reaction mixture is stirred for 16 hours at room temperature. The reaction is quenched with 0.5 mL water. The reaction mixture is stirred for ½ hour and 0.25 mL 15% NaOH (aq) is added. The reaction mixture is stirred for 1 hour, then 1 mL water is added and stirring is continued for another hour. The mixture is filtered, dried with MgSO4 and concentrated in vacuo to give the title compound, which is used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07534791B2 |
| 出典データセット | uspto-grants-2009_05 |
| ORD ID | ord-f8d83c6e9aa34f75b5047f67cabcd8a6 |
| 出典メモ | uspto-grants-2009_05 |