関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2,5-bis-(hydroxymethyl)-N-benzylimidazole | HCID 14316754 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Acetate | HCID 175 | — |
| 生成物 | 2-acetoxymethyl-5-hydroxymethyl-N-benzylimidazole | HCID 68617989 | — |
反応手順
To a solution of 2,5-bis-(hydroxymethyl)-N-benzylimidazole (436 mg, 2.0 mmol) in dichloromethane (10 mL) was added triethylamine (0.35 mL, 2.0 mmol) and acetic anhydride (0.19 mL, 2.0 mmol). The mixture was then stirred overnight (16 h) at room temperature. The reaction was then washed with aqueous ammonium chloride and the layers separated. The aqueous layer was extracted twice with dichloromethane. The combined organic fractions were then dried over anhydrous sodium sulfate and concentrated. Purification by chromatography on silica gel (5% methanol in dichloromethane) gave the monoacetate, 2-acetoxymethyl-5-hydroxymethyl-N-benzylimidazole, as a white powder (300 mg, 58%). 1H NMR (CDCl3) δ 1.83 (s, 3H), 4.49 (s, 2H), 5.06 (s, 2H), 5.33 (s, 2H), 6.97 (m, 2H), 7.28 (m, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07807694B2 |
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| 出典データセット | uspto-grants-2010_10 |
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| ORD ID | ord-4c45b45cfde047e9b4e95587b56a78ab |
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| 出典メモ | uspto-grants-2010_10 |
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