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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793467Generated: November 1, 2026

P-Anisidine → HCID 10403806, compound

https://huagongshe.com/reaction/1793467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Naphthyloxy)-1-chlorobutaneHCID 11658711—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 10403806HCID 10403806—

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of anhydrous potassium carbonate (10 gm, in excess) and p-anisidine (0.4 gm, 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 130° 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 as oily compound which was later crystallized by benzene hexane to get N-(4-methoxyphenyl)-[4-(naphthalen-2-yloxy)butyl]amine, yellow solid, m.p 95° C., (yield 0.67 gm, 97.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081465B2
Source datasetuspto-grants-2006_07
ORD IDord-c1e4717643944f04b05d68febe48cea9
Source noteuspto-grants-2006_07