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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490098Generated: November 1, 2026

(2-Acetamidophenyl) cyclohexyl methanone → (2-Aminophenyl)(cyclohexyl)methanone

https://huagongshe.com/reaction/1490098

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Acetamidophenyl) cyclohexyl methanoneHCID 11586813—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Product(2-Aminophenyl)(cyclohexyl)methanoneHCID 1563473391.1%

Reaction Steps

A solution of (2-acetamidophenyl) cyclohexyl methanone (0.53 g) in methanol (5 ml) and concentrated hydrochloric acid (15 ml) was heated at 80° C. for 1 hour. After this time the solution was cooled to ambient temperature and the solvents removed in vacuo. The residue was dissolved in water (10 ml) and basified with 4N sodium hydroxide solution (20 ml). The mixture was then extracted into ethyl acetate (4×20 ml) and the organic layers combined and dried (MgSO4). The solvent was evaporated and the residue chromatographed on silica gel using petrol:ethyl acetate (2:1), to afford the title compound (0.40 g) as a solid. The spectroscopic properties of this material were identical to those described in Method A.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05681833
Source datasetuspto-grants-1997_10
ORD IDord-dc748a3bf96d4ed99180ec254ab8785e
Source noteuspto-grants-1997_10