戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 7694作成日:2026年10月24日

Trimethylsilyl cyanide → [4-(1,3-Benzoxazol-2-yl)-2-(trifluoromethyl)phenyl]acetonitrile

https://huagongshe.com/ja/reaction/7694

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethylsilyl cyanideHCID 82115—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物2-[4-(Bromomethyl)-3-(trifluoromethyl)phenyl]-1,3-benzoxazoleHCID 21990977—
溶媒AcetonitrileHCID 6342—
生成物[4-(1,3-Benzoxazol-2-yl)-2-(trifluoromethyl)phenyl]acetonitrileHCID 10125560—

反応手順

To a suspension of 2-[4-(bromomethyl)-3-(trifluoromethyl)phenyl]-1,3-benzoxazole (528 mg, 1.5 mmol) and cyanotrimethylsilane (0.30 mL, 2.2 mmol) in acetonitrile (19 mL) was added TBAF (1.0M in THF, 2.2 mL, 2.2 mmol) and the mixture was stirred at rt for 2 h. The solvent was removed in vacuo and the crude was purified by flash chromatography eluting with EtOAc:hexanes (1:9) to afford the desired [4-(1,3-benzoxazol-2-yl)-2-(trifluoromethyl)phenyl]acetonitrile as a colorless solid. 1H NMR (CDCl3, 300 MHz) δ 8.60 (s, 1H), 8.48 (d, 1H), 7.88 (d, 1H), 7.82 (m, 1H), 7.63 (m, 1H), 7.43 (m, 2H), 4.05 (s, 2H). MS (ESI) 303 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087601B2
出典データセットuspto-grants-2006_08
ORD IDord-26845d3d550d49b5a8a35ee75d6d3a4d
出典メモuspto-grants-2006_08