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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352873Generated: November 1, 2026

Triethylamine → 1-allyl-N-(3-ethylphenyl)-1H-pyrrole-2-carboxamide

https://huagongshe.com/reaction/1352873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-EthylanilineHCID 11475—
ReactantBis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
ReactantPotassium bisulfateHCID 516920—
Reactant1-(prop-2-en-1-yl)-1H-pyrrole-2-carboxylic acidHCID 45082008—
SolventDichloromethaneHCID 6344—
Product1-allyl-N-(3-ethylphenyl)-1H-pyrrole-2-carboxamideHCID 2292868750.3%

Reaction Steps

A mixture of 1-allyl-1H-pyrrole-2-caboxylic acid (270 mg, 1.79 mmol), m-ethylaniline (0.43 g, 2.48 mmol), BOP-Cl (500 mg, 1.96 mmol) and triethylamine (210 mg, 2.08 mmol) in dichloromethane (3 ml) was stirred for 2 hours at room temperature. To the reaction mixture was added an aqueous 5% potassium hydrogensulfate solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water, an aqueous saturated sodium hydrogencarbonate solution and an aqueous saturated sodium chloride solution, and dried over magnesium sulfate. The solvent was removed and the residue was purified with silica gel chromatography (hexane:ethyl acetate=5:1→3:1) to give the subject compound (229 mg, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220773B2
Source datasetuspto-grants-2007_05
ORD IDord-66308b2ef61e4ea69cc21d7056b756be
Source noteuspto-grants-2007_05