戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 561017作成日:2026年10月26日

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

https://huagongshe.com/reaction/561017

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物1-Butanaminium, N,N,N-tributyl-, azideHCID 5743232—
反応物1,4-Cyclohexadiene-1,2-dicarbonitrileHCID 20439962—
反応物1-(6-Fluoropyridin-3-yl)ethan-1-olHCID 66600166—
溶媒DichloromethaneHCID 6344—
生成物5-(1-Azidoethyl)-2-fluoropyridineHCID 8664049265.8%

反応手順

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+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063212B2
出典データセットuspto-grants-2011_11
ORD IDord-560b8f80d2454092b3134c53b19523fa
出典メモuspto-grants-2011_11