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Potassium Carbonate → 2-n-Butyl-1-pivalyloxymethylimidazole-5-aldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Chloromethyl pivalate | HCID 87885 | — |
| 反応物 | 2-Butyl-5-formylimidazole | HCID 2735671 | — |
| 触媒 | HCID 178418406 | HCID 178418406 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-n-Butyl-1-pivalyloxymethylimidazole-5-aldehyde | HCID 19387327 | — |
反応手順
A suspension of 2-butylimidazol-5-aldehyde (16,92 g, 0.111 mol, prepared by manganese dioxide oxidation of the alcohol, prepared in Example 1,Method 2), chloromethyl pivalate (21.77 g, 0.145 mol), and potassium carbonate (20.07 g, 0.145 mol) in 200 ml of dimethylformamide was stirred at ambient temperature under argon for four days. The solids were removed by filtration and washed with ether. The combined filtrates were partitioned between diethyl ether and water. The ether phase was washed successively with water and brine, dried over magnesium sulfate and concentrated under vaccum to give 23.6 g of 2-n-butyl-1-pivalyloxymethylimidazole-5-aldehyde.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05418250 |
| 出典データセット | uspto-grants-1995_05 |
| ORD ID | ord-826ff577303045ea8be54312b21db837 |
| 出典メモ | uspto-grants-1995_05 |