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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283579Generated: October 30, 2026

Triethylamine → (E)-N-(2-azidoethyl)-2-methyl-3-phenylacrylamide

https://huagongshe.com/reaction/2283579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthylamine, 2-azido-HCID 55649—
ReactantOxalyl chlorideHCID 65578—
Reactantalpha-Methylcinnamic acidHCID 637817—
SolventDichloromethaneHCID 6344—
Product(E)-N-(2-azidoethyl)-2-methyl-3-phenylacrylamideHCID 5791435596.2%

Reaction Steps

To a 25 mL round-bottomed flask equipped with a magnetic stir bar was added (E)-2-methyl-3-phenylacrylic acid (0.0.512 g, 3.15 mmol) and dichloromethane (10 mL). Oxalyl chloride (0.400 g, 3.15 mmol) was added dropwise to the reaction mixture and allowed to stir for one hour. Then, the reaction mixture was concentrated de vacuo. To the crude mixture was then added dichloromethane (10 mL), 2-azidoethanamine (0.299 g, 3.47 mmol) and then triethylamine (0.351 g, 3.47 mmol) and allowed to stir for two hours. The reaction mixture was then concentrated de vacuo and then purified via silica gel column chromatography (100% dichloromethane to 1:40 methanol:dichloromethane) to give (E)-N-(2-azidoethyl)-2-methyl-3-phenylacrylamide (0.698 g, 96% yield). 1H NMR (300 MHz, CDCl3) δ 7.39 (m, 6H), δ 7.01 (s, 1H), δ 3.51 (t, 2H), δ 3.45 (t, 2H), δ 2.13 (s, 3H) ppm; 13C NMR (75 MHz, CDCl3) δ 170.5, 136.2, 134.5, 132.0, 130.3, 129.6, 128.9, 128.6, 128.3, 50.9, 39.8, 14.5 ppm; HRMS (ESI) calcd for C12H14N4O (M+) 230.1168. Found 230.1165.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145395B2
Source datasetuspto-grants-2015_09
ORD IDord-737c98788f874d9fb17a2bbab3bfdf56
Source noteuspto-grants-2015_09