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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235240Generated: October 30, 2026

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

https://huagongshe.com/reaction/235240

Reaction equation

Participants

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

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of (2-acetamidophenyl) cyclohexyl methanone (0.53 g, 2.16 mmol) in methanol (5 ml) and concentrated hydrochloric add (15 ml) was heated at 80° C. for 1 h. 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 amine (0.40 g, 91%) as a white solid. mp 73°-75° C. 1H NMR (360 MHz, CDCL3)-- 1.23-2.09 (10H, m), 3.27 (1H, m), 6.29 (2H, brs), 6.64 (2H, m), 7.25 (1H, dt, J=6 and 1 Hz), 7.76 (1H, dd, J -7 and 1 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597915
Source datasetuspto-grants-1997_01
ORD IDord-b1e787aae57f427598a3ad39411cde6d
Source noteuspto-grants-1997_01