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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8759생성일: 2026년 10월 24일

tert-Butyl 4-methoxy-4-(2-diazo-1,3-dioxopent-1-yl)piperidine-1-carboxylate → tert-Butyl 4-oxo-3-(1-oxoprop-1-yl)-1-oxa-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/ko/reaction/8759

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl 4-methoxy-4-(2-diazo-1,3-dioxopent-1-yl)piperidine-1-carboxylateHCID 73857865—
촉매Dirhodium tetraacetateHCID 152122—
용매Hydrochloric AcidHCID 313—
용매DichloromethaneHCID 6344—
생성물tert-Butyl 4-oxo-3-(1-oxoprop-1-yl)-1-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 2198389240.4%

반응 단계

A solution of rhodium acetate dimer (0.002 g, 0.005 mmol) in dichloromethane (27 mL) was heated to 81° C. A solution of tert-butyl 4-methoxy-4-(2-diazo-1,3-dioxopent-1-yl)piperidine-1-carboxylate (0.092 g, 0.270 mmol) from Step D in dichloromethane (7 mL) was added slowly dropwise over 12 min. The reaction mixture was refluxed for 45 min then poured into IN hydrochloric acid, and extracted three times with dichloromethane. 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 10% ethyl acetate/dichloromethane to afford the title compound (0.034 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091211B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-877888e2a7554dd4b0bc69673d1bcb3a
출처 메모uspto-grants-2006_08