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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1847779생성일: 2026년 10월 25일

Trifluoroacetic acid → (2-(Tert-butyl-dimethyl-silanyloxy)-ethyl]-(2-iodo-4-nitro-phenyl)-amine

https://huagongshe.com/reaction/1847779

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물2-Iodo-4-nitroanilineHCID 222629—
반응물2-((Tert-butyldimethylsilyl)oxy)acetaldehydeHCID 4187788—
반응물Sodium cyanoborohydrideHCID 5003444—
용매MethanolHCID 887—
생성물(2-(Tert-butyl-dimethyl-silanyloxy)-ethyl]-(2-iodo-4-nitro-phenyl)-amineHCID 5912939325%

반응 단계

To a solution of 2-iodo-4-nitroaniline (2.0 g, 7.6 mmol) and 2-(tert-butyldimethylsilyloxy)-acetaldehyde (3.5 g, 75% purity, 15 mmol) in methanol (30 mL) was added TFA (1.5 mL) at 0° C. The reaction mixture was stirred at this temperature for 30 min before NaCNBH3 (900 mg, 15 mmol) was added in portions. The mixture was stirred for 2 h and was then quenched with water. The resulting mixture was extracted with EtOAc (30 mL×3), the combined organic extracts were dried over anhydrous Na2SO4 and evaporated under vacuum, and the residue was purified by chromatography on silica gel (5% ethyl acetate/petroleum) to afford [2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-(2-iodo-4-nitro-phenyl)-amine (800 mg, 25%). 1H NMR (300 MHz, CDCl3) δ 8.57 (d, J=2.7 Hz, 1H), 8.12 (dd, J=2.4, 9.0 Hz, 1H), 6.49 (d, J=9.3 Hz, 1H), 5.46 (br s, 1H), 3.89 (t, J=5.4 Hz, 2H), 3.35 (q, J=5.4 Hz, 2H), 0.93 (s, 9H), 0.10 (s, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08952049B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-c04d05cdf05645d0aaed1738c8395766
출처 메모uspto-grants-2015_02