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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14311생성일: 2026년 10월 25일

Tetrahydrofuran → Tert-butyl 4-(trifluoromethanesulfonyloxy)-1,2,3,6-tetrahydropyridine-1-carboxylate

https://huagongshe.com/reaction/14311

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물1,1,1-Trifluoro-N-phenylmethanesulfonamideHCID 68012—
반응물tert-Butyl 2-oxopiperidine-1-carboxylateHCID 7577838—
반응물Lithium diisopropylamineHCID 45051747—
생성물Tert-butyl 4-(trifluoromethanesulfonyloxy)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 10991161—

반응 조건

온도0 °C

반응 단계

To a −70° C. stirred solution of N-Boc-piperidone (500 mg, 2.5 mmol) in tetrahydrofuran (11 mL) was added lithium diisopropylamine (1.37 mL of a 2 M solution in tetrahydrofuran, 2.75 mmol). The reaction mixture was stirred for 2 h, warmed to 0° C., and N-phenyltriflamide (955 mg, 2.67 mmol) was added. The solution was allowed to warm to room temperature and was stirred for 12 h. The reaction mixture was concentrated under reduced pressure. Purification by flash column chromatography (3:1 hexanes/ethyl acetate) afforded tert-butyl 4-{[(trifluoromethyl)sulfonyl]oxy}-3,6-dihydropyridine-1(2H)-carboxylate (240 mg): 1H NMR (300 MHz, CDCl3) δ 5.77 (s, 1H), 4.05 (m, 2H), 3.63 (m, 2H), 2.45 (m, 2H), 1.48 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-03f152eb106646e9b0d12632e1b86d0e
출처 메모uspto-grants-2010_06