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HRID 2361610作成日:2026年10月27日

Triethylamine → (E)-3-(4-fluorophenyl)acryloyl azide

https://huagongshe.com/reaction/2361610

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物4-Fluorocinnamic acidHCID 1530234—
溶媒BenzeneHCID 241—
生成物(E)-3-(4-fluorophenyl)acryloyl azideHCID 8668326690.7%

反応手順

To a solution of (E)-3-(4-fluorophenyl)acrylic acid (25 g, 150 mmol) in benzene (120 mL) was added triethylamine (30.5 g, 301 mmol) followed by DPPA (41.4 g, 150 mmol) at room temperature. The reaction mass was stirred at the same temperature for 18 h. The solvent was evaporated under reduced pressure and the residue was diluted with water and extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to get crude compound. The crude compound was purified by conventional column chromatography (Silica gel, 60-120 mesh) using 10% ethyl acetate in pet ether as mobile phase to get the desired compound as a white solid (26 g, 90%). 1H NMR (400 MHz, CDCl3): δ ppm 7.73-7.69 (d, J=16 Hz, 1H), 7.55-7.51 (m, 2H), 7.11-7.07 (m, 2H), 6.36-6.32 (d, J=16 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08691757B2
出典データセットuspto-grants-2014_04
ORD IDord-96d31ba597a449f4b0d2b87a68965ea5
出典メモuspto-grants-2014_04