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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361610Generated: October 26, 2026

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

https://huagongshe.com/reaction/2361610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant4-Fluorocinnamic acidHCID 1530234—
SolventBenzeneHCID 241—
Product(E)-3-(4-fluorophenyl)acryloyl azideHCID 8668326690.7%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691757B2
Source datasetuspto-grants-2014_04
ORD IDord-96d31ba597a449f4b0d2b87a68965ea5
Source noteuspto-grants-2014_04