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Acetic Anhydride → (1-((4-Methylphenyl)sulfonyl)-1H-imidazol-5-yl)methyl acetate
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 | (1-((4-Methylphenyl)sulfonyl)-1H-imidazol-5-yl)methanol | HCID 382151 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | (1-((4-Methylphenyl)sulfonyl)-1H-imidazol-5-yl)methyl acetate | HCID 382152 | — |
反応手順
To a solution of 10 mmole of 1-tosylimidazol-5-ylmethanol in 10 ml of chloroform is added dropwise 20 mmole of triethylamine followed by the addition of 13 mmole of acetic anhydride over a period of 2 hours. Stirring is continued for 5 hours at 25° C. after which the solvent is removed under reduced pressure. The residue is partitioned between ethyl acetate and water. The organic phase is washed with sodium bicarbonate, dried over magnesium sulfate and evaporated under vacuo. Recrystallization of the residue from ethyl acetate yields 5-acetoxymethyl-1-tosylimidazole.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04221914 |
| 出典データセット | uspto-grants-1980_09 |
| ORD ID | ord-a3aec77526df4621ac4e8bf28147b8e9 |
| 出典メモ | uspto-grants-1980_09 |