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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207863Generated: October 31, 2026

Triethylamine → 3-(4-Bromophenyl)-N-methoxy-N-methylprop-2-enamide

https://huagongshe.com/reaction/2207863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactantp-Bromocinnamic acidHCID 99777—
SolventDichloromethaneHCID 6344—
Product3-(4-Bromophenyl)-N-methoxy-N-methylprop-2-enamideHCID 7137623579.6%

Reaction Steps

4-Bromocinnamic acid (28.3 g, 124.6 mmol), N,O-dimethylhydroxylamine hydrochloride (14.6 g, 149.6 mmol), HOBT (33.7 g, 249.3 mmol), EDAC (47.8 g, 249.3 mmol) and triethylamine (34.7 mL, 249.3 mmol) were added to dichloromethane (800.0 mL). The reaction mixture was stirred at room temperature for 16 hours, quenched with a saturated solution of ammonium chloride, and then extracted with dichloromethane three times. The combined extract was washed with brine, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a yellow liquid residue. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/2) to give 26.8 g of the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376420B2
Source datasetuspto-grants-2016_06
ORD IDord-579933cd42d942d9b70f440e031162a9
Source noteuspto-grants-2016_06