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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 993193생성일: 2026년 10월 24일

tert-Butanol → Benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/993193

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물Benzyl 4-isocyanatopiperidine-1-carboxylateHCID 2776273—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylateHCID 21981786—

반응 단계

A solution of 3.2 g (12.3 mmol) of (1-benzyloxycarbonylpiperidin-4-yl)isocyanate from Step A in 25 mL of DMF was slowly added to a suspension of CuCl3 in 25 mL of DMF and 12 mL of t-butanol. The reaction was stirred for 24 h and then diluted with water and extracted twice with 1:1 ether: ethyl acetate. 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 FC eluting with 20% ethyl acetate in hexanes to afford 685 mg of title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06472410B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-c69a86db3f494bc6af5f4ea6a6877d96
출처 메모uspto-grants-2002_10