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Diisobutylaluminum hydride → 5-(Hydroxymethyl)-1H-benzimidazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisobutylaluminum hydride | HCID 14487 | — |
| 反応物 | Ethyl 1H-benzimidazole-6-carboxylate | HCID 13505555 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 5-(Hydroxymethyl)-1H-benzimidazole | HCID 13505556 | — |
反応手順
To a cooled (0° C.) suspension of ethyl-benzimidazole-5-carboxylate (4.76 g, 25 mmol) in CH2Cl2 (100 mL) was added a 1 M solution of DIBAL in CH2Cl2 (100 mL) and the mixture was stirred for 4 h. The reaction was quenched by the sequential addition of MeOH (8 mL), 1M NaOH (16 mL), and 30% sodium potassium tartrate (40 mL). The mixture was warmed to RT and filtered, and the solid residue was washed with CH2Cl2. The filtrate was concentrated in vacuo to afford the title compound as a brown solid: 1H NMR (400 MHz, DMSO-d6): δ4.58 (s, 1H), 7.14 (m, 1H), 7.46 (s, 1H), 7.51 (m, 1H), 8.15 (s, 1H); HRMS (FAB) C8H9N2O calcd. 149.1723 (M+1). Found 149.1045.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06610701B2 |
| 出典データセット | uspto-grants-2003_08 |
| ORD ID | ord-2b7aeb2f4d7f40889c0149c021f90d69 |
| 出典メモ | uspto-grants-2003_08 |