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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793473Generated: October 31, 2026

Cyclohexylamine → HCID 22022376, compound

https://huagongshe.com/reaction/1793473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Naphthyloxy)-1-chlorobutaneHCID 11658711—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 22022376HCID 22022376—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of anhydrous potassium carbonate (10 gm, in excess) and cyclohexylamine (0.28 ml, 0.003 mole) was taken in dry DMSO (40 ml). Now 4-(2-naphthyloxy)1-chlorobutane (0.5 gm, 0.002 mole) was added in it. Reaction mixture was refluxed at 150° C. for 5 hrs and the reaction was completed as checked by TLC. Reaction mixture was poured in distilled water (60 ml) and extracted with ethyl acetate thrice. The organic layer was separated and concentrated to get oily compound which was later crystallized by benzene hexane to get N-cyclohexyl-[3-(naphthalen-2-yloxy)-butyl]amine, solid. m.p., 94° C., (yield 0.61 gm, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081465B2
Source datasetuspto-grants-2006_07
ORD IDord-0d26b68af0fc4534abf38b5d89464753
Source noteuspto-grants-2006_07