戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 911269作成日:2026年10月26日

4-Nitrobenzonitrile → Benzonitrile, 4-(2,2,2-trifluoro-1,1-dimethylethoxy)-

https://huagongshe.com/reaction/911269

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrobenzonitrileHCID 12090—
反応物Sodium hydrideHCID 24758—
反応物1,1,1-Trifluoro-2-methylpropan-2-olHCID 68182—
溶媒Diethyl EtherHCID 3283—
溶媒HexamethylphosphoramideHCID 12679—
生成物Benzonitrile, 4-(2,2,2-trifluoro-1,1-dimethylethoxy)-HCID 1344033625.2%

反応手順

Add 2-trifluoromethyl-2-propanol (3.4 g, 27 mmol) slowly to a slurry of sodium hydride (0.6 g, 60% in mineral oil, washed with hexane) in HMPA (5 mL) under nitrogen. Stir the slurry for 15 min and add a solution of 4-nitrobenzonitrile (2.0 g, 13.5 mmol) in HMPA (10 mL). Stir the resulting purple slurry at ambient temperature for 16 h, dilute with diethyl ether (100 mL) and wash with 5% aqueous HCl (30 mL). Separate the layers and extract the aqueous layer with diethyl ether (2×50 mL). Combine the organic extracts and concentrate in vacuo. Purify by chromatography on silica gel eluting with hexane/EtOAc (9:1 to 1:1) to obtain the desired intermediate (780 mg, 25%). GC-MS m/z: 229 (M+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08022062B2
出典データセットuspto-grants-2011_09
ORD IDord-d976a0521a8f4b87bac0519b7764704d
出典メモuspto-grants-2011_09