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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238503생성일: 2026년 10월 24일

6-Nitroindoline → 1-(1-Methyl(4-piperidyl))-6-nitroindoline

https://huagongshe.com/ko/reaction/238503

반응식

참여 물질

역할이름HCID투입량
반응물6-NitroindolineHCID 29757—
반응물1-Methyl-4-piperidoneHCID 74049—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매Acetic AcidHCID 176—
용매1,1-DichloroethaneHCID 6365—
생성물1-(1-Methyl(4-piperidyl))-6-nitroindolineHCID 18796623—

반응 단계

6-Nitroindoline (5 g) was dissolved in 200 mL of dichloroethane, N-methyl-4-piperidone (5 g) was added to the mixture, followed by 12 g NaBH(OAc)3 and 1 mL of glacial AcOH. The mixture was stirred at RT overnight. Saturated NaHCO3 solution (200 mL) was added to the reaction mixture and stirred for 1 h. The resulting mixture was separated by separation funnel, the organic layer was extracted once with saturated NaHCO3 solution and once with brine. The resulting organic layer was dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel with 2:1 EtOAc:MeOH to afford an orange oil. MS: 262 (M+1). Calc'd. for C14H19N3O2—261.32.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642624B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-7d1fd85e774f4ec59f2291df1b4171fd
출처 메모uspto-grants-2014_02