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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7694생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Trimethylsilyl cyanideHCID 82115—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물2-[4-(Bromomethyl)-3-(trifluoromethyl)phenyl]-1,3-benzoxazoleHCID 21990977—
용매AcetonitrileHCID 6342—
생성물[4-(1,3-Benzoxazol-2-yl)-2-(trifluoromethyl)phenyl]acetonitrileHCID 10125560—

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-26845d3d550d49b5a8a35ee75d6d3a4d
출처 메모uspto-grants-2006_08