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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1255840생성일: 2026년 10월 26일

1,8-Diazabicyclo(5.4.0)undec-7-ene → 3-[(1S)-1-azidoethyl]-5-bromopyridine

https://huagongshe.com/reaction/1255840

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물(R)-1-(5-bromopyridin-3-yl)ethanolHCID 68655864—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물3-[(1S)-1-azidoethyl]-5-bromopyridineHCID 8664186075%

반응 단계

To a solution of (1R)-1-(5-bromopyridin-3-yl)ethanol (10 mmol) in tetrahydrofuran (40 mL), cooled to 0° C., was added diphenylphosphoryl azide (4.3 mL, 20 mmol) in one portion followed by 1,8-diazabicyclo[5.4.0]undec-7-ene (3 mL, 20 mmol) dropwise over 30 minutes. After this time the reaction mixture was allowed to warm slowly to room temperature and was stirred overnight. The mixture was diluted with ethyl acetate (50 mL) and water (50 mL), the two phases separated and the aqueous phase extracted with ethyl acetate (3×50 mL). The combined organic phases were washed with brine (50 mL), dried (MgSO4) and concentrated under reduced pressure to give a black liquid which was purified by flash chromatography (silica, ethyl acetate/hexanes) to give 3-[(1S)-1-azidoethyl]-5-bromopyridine (1.7 g, 75%) as a colourless liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08461161B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-4db8b242fd664bfd922465040967c31a
출처 메모uspto-grants-2013_06