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Imidazole → (1r)-2-Imidazolyl-1-phenylethan-1-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Imidazole | HCID 795 | — |
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | (+)-Styrene oxide | HCID 114705 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (1r)-2-Imidazolyl-1-phenylethan-1-ol | HCID 69735309 | 32% |
反応手順
In a manner similar to that of Example 49, step 1, imidazole (2.83 g, 41.6 mmol) is dissolved in absolute ethanol (45 mL). Pyridine (0.11 mL) is added followed by addition of (R)-(+) styrene oxide (5.0 g, 41.6 mol, Aldrich Chemical Co.), followed by heating at reflux for 18 hours. The mixture is evaporated in vacuo to a syrup and suspended between ethyl ether (250 mL) and water (100 mL) to give a solid precipitate. The suspension is filtered and washed with ethyl ether. The solid is recrystallized from hot ethyl acetate and dried in vacuo (2.52 g, 32% yield). MS: APCI: M+1, 189.1 (M: 188.2). NMR spectrum is consistent with structure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06943183B2 |
| 出典データセット | uspto-grants-2005_09 |
| ORD ID | ord-150e80cf7b2f4adaa9053a82b1eba305 |
| 出典メモ | uspto-grants-2005_09 |