돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 911269생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/911269

반응식

참여 물질

역할이름HCID투입량
반응물4-NitrobenzonitrileHCID 12090—
반응물Sodium hydrideHCID 24758—
반응물1,1,1-Trifluoro-2-methylpropan-2-olHCID 68182—
용매Diethyl EtherHCID 3283—
용매HexamethylphosphoramideHCID 12679—
생성물Benzonitrile, 4-(2,2,2-trifluoro-1,1-dimethylethoxy)-HCID 1344033625.2%

반응 단계

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+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08022062B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-d976a0521a8f4b87bac0519b7764704d
출처 메모uspto-grants-2011_09