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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 887667생성일: 2026년 10월 26일

Trifluoroacetic anhydride → 2,2,2-Trifluoro-N-[2-(4-nitro-phenyl)-ethyl]-acetamide

https://huagongshe.com/reaction/887667

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic anhydrideHCID 9845—
반응물DiisopropylethylamineHCID 81531—
반응물Benzeneethanamine, 4-nitro-, hydrochloride (1:1)HCID 458983—
용매DichloromethaneHCID 6344—
생성물2,2,2-Trifluoro-N-[2-(4-nitro-phenyl)-ethyl]-acetamideHCID 6423744—

반응 단계

To a solution of 4-nitrophenethylamine hydrochloride (50 g, 0.247 mole), DIEA (128 mL, 0.74 mole, 3 eq.) and CH2Cl2 (500 mL) in a 1 L round bottom flask equipped with a magnetic stirrer was added (CF3CO)2O (52.5 mL, 0.37 mole, 1.5 eq) dropwise at 5-10° C. (with ice/water bath). After stirring for another 1 h after the addition at RT, the reaction was quenched with water (200 mL) and transferred into a separatory funnel. The organic layer was separated, washed with water and sat. NH4Cl, dried over Na2SO4, filtered, concentrated to give a brown oil. The crude was triturated with water (300 mL), filtered and dried on vacuum overnight to give the desired 2,2,2-trifluoro-N-[2-(4-nitro-phenyl)-ethyl]-acetamide as a yellow solid. This can be used for next step without further purification. An analytical sample was obtained through recrystallization from CH3OH/H2O as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08247430B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-b1f2ea9aff9a4066930400f85f987c56
출처 메모uspto-grants-2012_08