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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132858생성일: 2026년 10월 27일

Dimethylformamide dimethyl acetal → tert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylate

https://huagongshe.com/reaction/132858

반응식

참여 물질

역할이름HCID투입량
반응물Dimethylformamide dimethyl acetalHCID 78373—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
용매DimethylformamideHCID 6228—
생성물tert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylateHCID 53395404—

반응 단계

A solution of tert-butyl 4-oxo-1-piperidinecarboxylate (8.73 g, 44 mmol) and N,N-dimethylformamide dimethyl acetal (5.8 mL, 44 mmol) in 80 mL of dry N,N-dimethylformamide was warmed at 80° C. for 18 h. The solution was cooled and concentrated under reduced pressure, and the residue was partitioned between ethyl acetate and water. The mixture was filtered through a pad of Celite, and the organic layer was separated, washed with saturated brine, dried over magnesium sulfate and concentrated under reduced pressure to afford the title compound as an orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388019B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-eaf1fa1683814914835bc4295fe62e17
출처 메모uspto-grants-2008_06