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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19890생성일: 2026년 10월 25일

Triphenylphosphine → Tert-butyl 4-(3-methyl-4-nitrophenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/19890

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-Methyl-4-nitrophenolHCID 17412—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물Tert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(3-methyl-4-nitrophenoxy)piperidine-1-carboxylateHCID 18542679—

반응 단계

Diisopropyl azodicarboxylate (10.56 mL, 1.6 eq.) was added to a cold (0° C.) mixture of 3-methyl-4-nitrophenol (5 g, 1.0 eq.), 1-tert-butyloxycarbonyl-4-hydroxy-piperidine (9.96 g, 1.6 eq.) and triphenylphosphine (13.85 g, 1.6 eq.) in tetrahydrofuran (205 mL). After 1 h stirring, the mixture was evaporated to dryness and dissolved in tert-butylmethylether. The organic phase was washed with 0.5M sodium hydroxide solution and 5% sodium chloride solution, dried over sodium sulfate, filtered and evaporated to dryness. The product was recrystallized from methanol to yield 9.498 g (88%) as white crystals. MS (m/e): 336.2 (M, 10%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745479B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6faa8a0bc8f0409f90583664eb3f629d
출처 메모uspto-grants-2010_06