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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793471Generated: October 31, 2026

Cyclohexylamine → HCID 10445802, compound

https://huagongshe.com/reaction/1793471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Naphthyloxy)-1-chloroethaneHCID 349877—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 10445802HCID 10445802—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of anhydrous potassium carbonate (10 gm, in excess) and cyclohexylamine (0.32 ml, 0.003 mole) was taken in dry DMSO (40 ml). Now 2-(2-naphthyloxy)-1-chloro ethane (0.5 gm, 0.002 mole) was added in it. Reaction mixture was refluxed at 140° C. for 7 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-[2-(naphthalen-2-yloxy)-ethyl]amine, solid, m.p. 89° C., (yield 0.56 gm, 85.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081465B2
Source datasetuspto-grants-2006_07
ORD IDord-1a88f068295e44a0826659c21b8f3605
Source noteuspto-grants-2006_07