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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | ethyl (3R)-piperidine-3-carboxylate | HCID 185582 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | 7-(methoxymethoxy)-2H-chromene-3-carbaldehyde | HCID 58438729 | — |
| 용매 | 1,1-Dichloroethane | HCID 6365 | — |
| 생성물 | ethyl (3R)-1-{[7-(methoxymethoxy)-2H-chromen-3-yl]methyl}piperidine-3-carboxylate | HCID 58438698 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08193378B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-5af4ddab628246b4be6b910b01411837 |
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| 출처 메모 | uspto-grants-2012_06 |
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