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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217472생성일: 2026년 10월 24일

ethyl (3R)-piperidine-3-carboxylate → ethyl (3R)-1-{[7-(methoxymethoxy)-2H-chromen-3-yl]methyl}piperidine-3-carboxylate

https://huagongshe.com/ko/reaction/217472

반응식

참여 물질

역할이름HCID투입량
반응물ethyl (3R)-piperidine-3-carboxylateHCID 185582—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물7-(methoxymethoxy)-2H-chromene-3-carbaldehydeHCID 58438729—
용매1,1-DichloroethaneHCID 6365—
생성물ethyl (3R)-1-{[7-(methoxymethoxy)-2H-chromen-3-yl]methyl}piperidine-3-carboxylateHCID 58438698—

반응 조건

온도80 °C

반응 단계

To a solution of 7-(methoxymethoxy)-2H-chromene-3-carbaldehyde (5.00 g) and ethyl (3R)-piperidine-3-carboxylate (4.20 mL) in dichloroethane (150 mL) was added sodium triacetoxyborohydride (12.0 g), followed by stirring at 80° C. for 4 hours. The reaction liquid was cooled to room temperature and then saturated aqueous NaHCO3 was added thereto, followed by extraction with chloroform. The organic layer was washed with brine and dried over anhydrous sodium sulfate, and the vehicle was evaporated. The residue was purified by silica gel column chromatography (hexane:EtOAc=4:1) to obtain ethyl (3R)-1-{[7-(methoxymethoxy)-2H-chromen-3-yl]methyl}piperidine-3-carboxylate (7.30 g) as a yellow oily substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193378B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-5af4ddab628246b4be6b910b01411837
출처 메모uspto-grants-2012_06