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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793499Generated: November 1, 2026

P-Anisidine → HCID 10096933, compound

https://huagongshe.com/reaction/1793499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantHCID 85999797HCID 85999797—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 10096933HCID 10096933—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 2,6-bis(3-chloropropyloxy)naphthalene(1 gm, 0.003 mole) and p-anisidine(1.17 gm, 0.005 mole) was taken in 60 ml dry DMSO. It was refluxed at 140° C. for 12 hrs. The completion of the reaction was checked by TLC. The reaction mixture was poured into distilled water (80 ml) and extracted with ethyl acetate thrice. The organic layer was separated and concentrated to get oily compound which was further crystallized by benzene hexane to get the desired compound, m.p. 129° C., (yield 1.4 gm, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081465B2
Source datasetuspto-grants-2006_07
ORD IDord-8602afcfcfc34702adeae4b8cb6b6cad
Source noteuspto-grants-2006_07