Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831041Generated: October 30, 2026

4-Aminophenol → 2-Cyclohexyl-N-(4-hydroxy-phenyl)-acetamide

https://huagongshe.com/reaction/1831041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantPyridineHCID 1049—
ReactantCyclohexylacetyl chlorideHCID 2757989—
SolventDichloromethaneHCID 6344—
Product2-Cyclohexyl-N-(4-hydroxy-phenyl)-acetamideHCID 22047780—

Reaction Steps

To a solution of 4-aminophenol (3.83 g, 35.1 mmol) in dichloromethane (50 ml) were added cyclohexylacetyl chloride (11.26 g, 70.1 mmol) and pyridine (5.67 ml, 70.1 mmol), while cooling the reaction mixture in an ice bath. After the addition was completed, the cooling bath was removed and stirring was continued overnight at room temperature. The solvent was removed by evaporation and the residue was dissolved in THF (300 ml). 6N NaOH (aq, 41 ml) was added and the mixture was stirred at room temperature for 4 h. The solution was acidified with 1 N hydrochloric acid and the organic phase was removed by evaporation. The solid material was collected by filtration, dried and dissolved in methanol (100 ml). A solution of KOH (5.5 g) in methanol (50 ml) was added. After stirring for 1 h at room temperature water (200 ml) was added and the organic solvent was removed by evaporation. The aqueous phase was acidified with 1 N HCl. The title product was isolated by filtration and dried in vacuo (6.31 g, 77%, pink crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067517B2
Source datasetuspto-grants-2006_06
ORD IDord-4ea37a6a41b34676a34237ff9a21a33b
Source noteuspto-grants-2006_06