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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448730Generated: October 25, 2026

Furfuryl Alcohol → 1-[[(2-Furanylmethoxy)carbonyl]amino]cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/reaction/448730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuryl AlcoholHCID 7361—
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantMethyl 1-aminocyclohexanoateHCID 4048819—
SolventTolueneHCID 1140—
Product1-[[(2-Furanylmethoxy)carbonyl]amino]cyclohexanecarboxylic acid methyl esterHCID 5767288888.1%

Reaction Steps

3.67 g (30 mmol) of dimethylaminopyridine was added to a solution of 65.48 g (0.3 mol) of di-t-butyl dicarbonate in 300 ml of anhydrous toluene, and the mixture was stirred at room temperature for 15 minutes. A solution of 47.17 g (0.3 mol) of 1-aminocyclohexanecarboxylic acid methyl ester in 100 ml of anhydrous toluene was added to the reaction solution, and the mixture was stirred at room temperature for 1 hour. Further, after 60.71 g (0.6 mol) of triethylamine and 44.1 g (0.45 mol) of furfuryl alcohol were added, the mixture was heated under reflux for 3 hours. The reaction solution was returned to room temperature and was concentrated under reduced pressure. The obtained residue was crushed by a mortar, and it was stirred in a mixture solution of 5 ml of hydrochloric acid and 3 L of water for 18 hours. The obtained crystal was collected by filtration to obtain 74.37 g (88%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481725B2
Source datasetuspto-grants-2013_07
ORD IDord-7cbbf8d9e18e419fbc2b42a30e8de1e8
Source noteuspto-grants-2013_07