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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | tert-Butyl 4-((2-bromo-2,2-difluoroacetamido)methyl)-4-hydroxypiperidine-1-carboxylate | HCID 57988980 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | tert-Butyl 2,2-difluoro-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08629271B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-f7fcc2248e7f413a9a54d7499ae4b8db |
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| 출처 메모 | uspto-grants-2014_01 |
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