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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 471049생성일: 2026년 10월 25일

Potassium tert-butoxide → tert-Butyl 2,2-difluoro-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate

https://huagongshe.com/reaction/471049

반응식

참여 물질

역할이름HCID투입량
반응물Potassium tert-butoxideHCID 23665647—
반응물tert-Butyl 4-((2-bromo-2,2-difluoroacetamido)methyl)-4-hydroxypiperidine-1-carboxylateHCID 57988980—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl 2,2-difluoro-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylateHCID 57989103—

반응 단계

A solution of tert-butyl 4-((2-bromo-2,2-difluoroacetamido)methyl)-4-hydroxypiperidine-1-carboxylate (example 37, step a) (3.2 g) in THF (40 mL) was added dropwise over 15 minutes to a stirred solution of potassium tert-butoxide (1M in t-butanol, 16.53 mL) and THF (60 mL) at 70° C. under nitrogen. At the end of the addition the mixture was heated for a further 10 minutes and then cooled to room temperature. The mixture was partitioned between ethyl acetate and brine, the organic layer was dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure. The crude product was purified by flash silica chromatography using 30% isohexane in ethyl acetate. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 0.55 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629271B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-f7fcc2248e7f413a9a54d7499ae4b8db
출처 메모uspto-grants-2014_01