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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 561017생성일: 2026년 10월 25일

Triphenylphosphine → 5-(1-Azidoethyl)-2-fluoropyridine

https://huagongshe.com/reaction/561017

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물1-Butanaminium, N,N,N-tributyl-, azideHCID 5743232—
반응물1,4-Cyclohexadiene-1,2-dicarbonitrileHCID 20439962—
반응물1-(6-Fluoropyridin-3-yl)ethan-1-olHCID 66600166—
용매DichloromethaneHCID 6344—
생성물5-(1-Azidoethyl)-2-fluoropyridineHCID 8664049265.8%

반응 단계

To a 1-L flask kept cold in a ice bath, add triphenylphosphine (27.9 g, 106.3 mmol), 1,4-cyclohexadiene-1,2-dicarbonitrile, 4,5-dichloro-3,6-dioxo-(24.12 g, 106.3 mmol). Add dichloromethane slowly with stirring (150 mL). To the dark solution add tetra-N-butylammonium azide (30.23 g, 106.3 mmol) slowly, followed by 1-(6-fluoro-pyridin-3-yl)-ethanol (10 g, 70.85 mmol) dissolved in dichloromethane (10 mL). Remove the flask from the ice bath and stir at room temperature for 1 hour. Remove the solvent on a rotovap and purify by normal phase chromatography 5% to 20% ethyl acetate in hexanes to obtain the product as colorless oil (7.75 g). GCMS (EI) m/z 166 M+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063212B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-560b8f80d2454092b3134c53b19523fa
출처 메모uspto-grants-2011_11