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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130882Generated: October 25, 2026

Methanol → 2-(4-Methoxyphenethylamino)cyclohexanol

https://huagongshe.com/reaction/130882

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 CH2Cl2 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/CH2Cl2/2.0 M NH3 in MeOH to afford 2-(4-methoxyphenethylamino)cyclohexanol. (1.38 g, 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381719B2
Source datasetuspto-grants-2008_06
ORD IDord-02ecfa8e9a624065a593c932350603ad
Source noteuspto-grants-2008_06