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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8756생성일: 2026년 10월 23일

Propanal → tert-Butyl 4-(3-hydroxy-1-oxopent-1-yl)-4-methoxypiperidine-1-carboxylate

https://huagongshe.com/ko/reaction/8756

반응식

참여 물질

역할이름HCID투입량
반응물PropanalHCID 527—
반응물Ammonium ChlorideHCID 25517—
반응물Tert-butyl 4-acetyl-4-methoxypiperidine-1-carboxylateHCID 21983927—
반응물Lithium diisopropylamineHCID 45051747—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl 4-(3-hydroxy-1-oxopent-1-yl)-4-methoxypiperidine-1-carboxylateHCID 2198400455.9%

반응 단계

To a solution of tert-butyl 4-acetyl-4-methoxypiperidine-1-carboxylate (0.589 g, 2.29 mmol) from Step A in tetrahydrofuran (20 mL) at −78° C. was added lithium diisopropylamine (0.650 mL, 0.974 mmol) followed by propionaldehyde (0.266 g, 0.330 mL, 4.58 mmol). After 5 min, the reaction mixture was poured into saturated ammonium chloride, and extracted three times with diethyl ether. The organic layers were combined, washed with saturated sodium chloride solution, dried over sodium sulfite, filtered, and concentrated. The residue was purified by flash chromatography eluting with 40% ethyl acetate/hexanes to afford the title compound (0.404 g). MS/EI (acetonitrile/water): m/z 216.1 (M+1−BOC) retention time=2.69 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091211B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b89820f3efd14138aa3a6cb136df92cc
출처 메모uspto-grants-2006_08