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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42631생성일: 2026년 10월 25일

Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine → 4-[1-Benzyl-3-(trifluoromethyl)pyrrolidin-3-yl]-2,6-bis(trifluoromethyl)pyridine

https://huagongshe.com/reaction/42631

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
반응물2,6-Bis(trifluoromethyl)-4-(3,3,3-trifluoroprop-1-en-2-yl)pyridineHCID 86664621—
촉매Trifluoroacetic acidHCID 6422—
용매DichloromethaneHCID 6344—
생성물4-[1-Benzyl-3-(trifluoromethyl)pyrrolidin-3-yl]-2,6-bis(trifluoromethyl)pyridineHCID 8667492685%

반응 단계

To the solution of 2,6-bis(trifluoromethyl)-4-(3,3,3-trifluoroprop-1-en-2-yl)pyridine (1.25 g) and N-benzyl-1-methoxy-N-[(trimethylsilyl)methyl]methanamine (5.0 g) in dichloromethane was added dropwise the solution of trifluoroacetic acid (0.038 g) in dichloromethane while cooling with ice. On completion of the dropwise addition, the mixture was warmed to room temperature and stirred over night. The mixture was washed with saturated sodium bicarbonate water and dried over anhydrous magnesium sulfate. After the drying agent was filtered off, the solvent was distilled away under the reduced pressure, and the residue was then purified by silica gel chromatography to yield 4-[1-benzyl-3-(trifluoromethyl)pyrrolidin-3-yl]-2,6-bis(trifluoromethyl)pyridine (1.52 g). 1H-NMR (CDCl3) δ: 2.23-2.29 (1H, m), 2.65-2.69 (2H, m), 2.96 (1H, d), 3.05-3.15 (2H, m), 3.58 (1H, d), 3.82 (1H, d), 7.26-7.37 (5H, m), 8.00 (2H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536201B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-838af80dacb64276b9baca66c568568e
출처 메모uspto-grants-2013_09