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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793498Generated: November 1, 2026

P-Anisidine → HCID 11755168, compound

https://huagongshe.com/reaction/1793498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantHCID 22022382HCID 22022382—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 11755168HCID 11755168—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 2,7-bis(3-chloropropyloxy)naphthalene (1 gm, 0.003 mole) and p-anisidine (1.17 gm, 0.005 mole) were 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 as solid, m.p. 127° C., (yield 1.34 gm, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081465B2
Source datasetuspto-grants-2006_07
ORD IDord-20916a283f7b4e35ae8b97c1acc5e84b
Source noteuspto-grants-2006_07