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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 369994생성일: 2026년 10월 25일

Water → 1,1-Dimethylethyl 4-azido-1-piperidinecarboxylate

https://huagongshe.com/reaction/369994

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium AzideHCID 33557—
반응물Sodium BicarbonateHCID 516892—
반응물tert-Butyl 4-bromopiperidine-1-carboxylateHCID 15541517—
촉매Sodium IodideHCID 5238—
용매DimethylformamideHCID 6228—
생성물1,1-Dimethylethyl 4-azido-1-piperidinecarboxylateHCID 11458794100.2%

반응 단계

To a solution of 45.3 g (172 mmol) of 4-bromo-1-(tert-butoxycarbonyl)piperidine in 750 mL of DMF was added 22.3 g (343 mmol) of sodium azide and 2.5 g (17 mmol) of sodium iodide. The reaction was stirred at RT for 24 h and then at 60° C. for 4 h. The mixture was poured into water containing 20 mL of sodium bicarbonate and extracted twice with 1:1 ether/hexane. The organic layers were each washed with a portion of water and brine, dried over sodium sulfate, combined and concentrated. The residue was purified by flash column chromatography, eluting with 5-10% ethyl acetate in hexane, to afford 39 g of title compound having a trace of elimination byproduct. 1H NMR (400 MHz, CDCl3): δ 3.78 (m, 2H), 3.55 (m, 1H), 3.07 (m, 2H), 1.85 (m, 2H), 1.52 (m, 2H), 1.43 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06140349
출처 데이터셋uspto-grants-2000_10
ORD IDord-5d1170d8c5934c1dba6fb9f33ddcb659
출처 메모uspto-grants-2000_10