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Sodium borohydride → Chloro-4-(4-(2-nitroethyl)phenoxy)-2-(trifluoromethyl)benzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | (E)-1-Chloro-4-(4-(2-nitrovinyl)phenoxy)-2-(trifluoromethyl)benzene | HCID 67775160 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Chloro-4-(4-(2-nitroethyl)phenoxy)-2-(trifluoromethyl)benzene | HCID 67775633 | 174.1% |
反応手順
To a suspension of (E)-1-chloro-4-(4-(2-nitrovinyl)phenoxy)-2-(trifluoromethyl)benzene (13 g, 43.2 mmol) and silica gel (120 g, 100-200 Mesh) in i-PrOH (155 mL) and CHCl3 (465 mL), was added NaBH4 (13.65 g, 361 mmol) portionwise. The reaction mixture was stirred overnight at rt, filtered, and washed with DCM (1 L). The organic phase was washed with sat. NaHCO3 (200 mL), then brine, and dried over anhydrous Na2SO4 and concentrated to afford the title compound as a brown liquid (26 g, 50% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09273054B2 |
| 出典データセット | uspto-grants-2016_03 |
| ORD ID | ord-fe4a9b24104248f488989a7e462047fa |
| 出典メモ | uspto-grants-2016_03 |