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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1696320생성일: 2026년 10월 26일

Hydrochloric Acid → 2-Fluoro-5-neopentylpyridine

https://huagongshe.com/reaction/1696320

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물5-Bromo-2-fluoropyridineHCID 2783168—
반응물HCID 178418809HCID 178418809—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
용매1,4-DioxaneHCID 31275—
생성물2-Fluoro-5-neopentylpyridineHCID 57515845—

반응 단계

To a stirred, cooled (−78° C.) solution of (1S,5S)-9-methoxy-9-bora-bicyclo[3.3.1]nonane (260 ml, 260 mmol) in THF (200 ml) was added neopentylmagnesium chloride (260 ml, 260 mmol) drop-wise. The mixture slowly warmed to RT and stirred for 3 h. The white solid was filtered off and washed thoroughly with pentane. The filtrate was concentrated to give the light yellow oil. This residue was diluted with p-dioxane (300 ml) and to this was added 5-bromo-2-fluoropyridine (35.20 g, 200 mmol), (Ph3P)4Pd (9.7 g, 8.4 mmol), and 5 N NaOH (168 ml, 838 mmol). The resulting reaction mixture was heated at 95° C. in 16 h. The mixture was cooled and added 5 N HCl (168 ml) and the reaction was stirred for 1 h and extracted with ether (3×). The organic layers were washed with brine, dried over MgSO4, concentrated and purified by ISCO (5% EtOAc/Hexanes) to give the light yellow oil. MS (m+1): 168.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08163766B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-e19902714dce47958481a9252dc33653
출처 메모uspto-grants-2012_04