化工社化工社 化学情報印刷レポート · 研究参考用
Ammonia → 2-(dimethoxymethyl)-5-methyl-4-(trifluoromethyl)-1H-imidazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Chlorosuccinimide | HCID 31398 | — |
| 反応物 | Acetaldehyde, 2,2-dimethoxy- | HCID 162650 | — |
| 反応物 | 2,2,2-Trifluoro-1-(2-methyl-1,3-dithian-2-yl)ethanone | HCID 86648480 | — |
| 触媒 | Silver Nitrate | HCID 24470 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 2-(dimethoxymethyl)-5-methyl-4-(trifluoromethyl)-1H-imidazole | HCID 67549218 | — |
反応手順
NCS (870 mg, 6.51 mmol) and silver nitrate (1.48 g, 8.71 mmol) were dissolved in acetonitrile (40 mL) and distilled water (10 mL). 2,2,2-Trifluoro-1-(2-methyl-1,3-dithian-2-yl)ethanone obtained in Example (36a) (500 mg, 2.17 mmol) was added, and the mixture was stirred for 40 minutes. Thereafter, dimethoxyacetaldehyde (5.76 M aqueous solution, 0.4 mL, 23.0 mmol) and 28% aqueous ammonia (2 mL) were added, and the mixture was stirred at room temperature for 18 hours. The reaction solution was filtered through celite and then concentrated under reduced pressure. The resulting compound was used for the next reaction without purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08536197B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-3540bec67c3547b392f9605095eb2780 |
| 出典メモ | uspto-grants-2013_09 |