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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73534생성일: 2026년 10월 23일

Sodium Bicarbonate → (S)-benzyl 3-(tert-butoxycarbonylamino)-5-ethylidenepiperidine-1-carboxylate

https://huagongshe.com/ko/reaction/73534

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물Potassium tert-butoxideHCID 23665647—
반응물HCID 68922849HCID 68922849—
촉매Phosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
용매TetrahydrofuranHCID 8028—
생성물(S)-benzyl 3-(tert-butoxycarbonylamino)-5-ethylidenepiperidine-1-carboxylateHCID 68922866—

반응 조건

온도0 °C

반응 단계

To a suspension of ethyltriphenylphosphonium bromide (11 eq) in 14 mL of THF was added potassium tert-butoxide (10 eq) at room temperature. The reaction mixture was stirred at that temperature for 20 minutes. Then the reaction was cooled to 0° C., and (S)-benzyl 3-(tert-butoxycarbonylamino)-5-oxopiperidine-1-carboxylate (1 eq) in 7 mL of THF was added to the reaction mixture. The reaction was allowed to warm up room temperature. After being stirred for 40 minutes, the reaction mixture was poured into aq. sodium bicarbonate and extracted with ethyl acetate. The organic layer was separated and washed with brine, then dried over anhydrous MgSO4, filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (EtOAc:hexanes=2:1) to yield (S)-benzyl 3-(tert-butoxycarbonylamino)-5-ethylidenepiperidine-1-carboxylate. LC/MS (m/z): 261.2 (MH+-100), Rt:1.12 min. HPLC: Rt:4.31 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829193B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e6f8476ce6314680b863fca27c4338a2
출처 메모uspto-grants-2014_09