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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627439Generated: October 26, 2026

Triethylamine → 1-[(3-Furanylcarbonyl)amino]cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/reaction/1627439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Furoic acidHCID 10268—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantMethyl 1-aminocyclohexane-1-carboxylate hydrochlorideHCID 22645079—
SolventDichloromethaneHCID 6344—
Product1-[(3-Furanylcarbonyl)amino]cyclohexanecarboxylic acid methyl esterHCID 3247401091%

Reaction Steps

105 g (550 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added to a solution of 98.8 g (500 mmol) of 1-aminocyclohexanecarboxylic acid methyl ester hydrochloride, 84.2 g (550 mmol) of 1-hydroxybenzotriazole, 56.0 g (500 mmol) of 3-furancarboxylic acid and 152 g (1.5 mol) of triethylamine in 1000 ml of methylene chloride under ice-cooling. After the mixture was stirred at room temperature overnight, the reaction solution was concentrated under reduced pressure. Ethyl acetate was added to the residue, and the mixture was successively washed with water, a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with anhydrous sodium sulfate. After the solvent was distilled off under reduced pressure, the obtained crystal was washed with diisopropyl ether to obtain 114 g (91%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785631B2
Source datasetuspto-grants-2014_07
ORD IDord-6c37fe921e314f89b791b2d18d4da163
Source noteuspto-grants-2014_07