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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228334Generated: October 25, 2026

Methanol → 2-(4-Methoxyphenethylamino)cyclohexanol

https://huagongshe.com/reaction/228334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
Reactant2-AminocyclohexanolHCID 23286—
Reactant4-(2-Chloroethyl)phenyl methyl etherHCID 87513—
SolventDimethylformamideHCID 6228—
Product2-(4-Methoxyphenethylamino)cyclohexanolHCID 60714650—

Reaction Conditions

Temperature100 °C

Reaction Steps

Mix (±)-2-aminocyclohexanol (1.5227 g, 13.2 mmol), K2CO3 (4.56 g, 33.0 mmol), and 1-(2-chloroethyl)-4-methoxybenzene (2.0 mL, 13.2 mmol) in DMF (30 mL). Heat at 100° C. for 24 hours. Cool down to room temperature and filtrate with MeOH wash. Concentrate and remove DMF azeotropically with xylenes. Take up the residue in CH2C2 and H2O (100 mL each). Separate the layers and extract the aqueous layer with CH2Cl2 (2×100 mL). Wash the organic layers with H2O and brine (100 mL each). Dry the combined organic layers over MgSO4, concentrate and purify by flash chromatography, eluting with 50:45:5 EtOAc/CH2Cl/2.0 M NH3 in MeOH to afford 2-(4-methoxyphenethylamino)cyclohexanol. (1.38 g, 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560463B2
Source datasetuspto-grants-2009_07
ORD IDord-7b727e9032f0430099b8f30e0642387b
Source noteuspto-grants-2009_07