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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 590778생성일: 2026년 10월 25일

Trifluoroacetic acid → 1-Benzyl-3-nitro-4-phenylpyrrolidine

https://huagongshe.com/reaction/590778

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Benzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
반응물beta-nitrostyrene, (E)-HCID 5284459—
용매DichloromethaneHCID 6344—
생성물1-Benzyl-3-nitro-4-phenylpyrrolidineHCID 58009180—

반응 단계

To a solution of (E)-(2-nitrovinyl)benzene (110 g, 0.738 mol) and TFA (8.42 g, 0.073 mol) in DCM (500 mL) was added N-benzyl-1-methoxy-N-((trimethylsilyl)methyl)-methanamine (351.4 g, 1.476 mol) in DCM (500 mL) drop-wise at 0° C. for a period of 30 min. Then the reaction mixture was stirred at room temperature for 48 h. After completion of the reaction, the mixture was concentrated in vacuo, dissolved in water, and extracted into EtOAc (×2, 1.0 L). The organic layer was separated, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue was purified via flash chromatography (20-80% petroleum ether/EtOAc) to afford (3S and R, 4R and S)-1-benzyl-3-nitro-4-phenylpyrrolidine. MS ESI calc'd. For C17H18N2O2 [M+1]+ 283. found 283.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09233979B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-61ee15ffb2a74b249eb2cacf9d013f34
출처 메모uspto-grants-2016_01