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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634862Generated: October 31, 2026

N-methyl-2-pyrrolidone → HCID 59620855, compound

https://huagongshe.com/reaction/1634862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium amideHCID 24533—
Reactantp-Vinylbenzyl chlorideHCID 74126—
Reactant1-PentylnaphthaleneHCID 518732—
Catalyst2,5-Di-tert-butylhydroquinoneHCID 2374—
CatalystSodium IodideHCID 5238—
SolventChloroformHCID 6212—
ProductHCID 59620855HCID 5962085577.1%

Reaction Steps

Into 120 g of N-methyl-2-pyrrolidone were dissolved 11.5 g of 1-amylnaphthalene, and then 3.74 g of sodium amide were added to the resultant solution while the solution was stirred at room temperature. Into the solution were added 1.20 g of sodium iodide as a catalyst and 0.89 g of 2,5-di-t-butylhydroquinone as a polymerization inhibitor. Thereafter, 13.4 g of p-chloromethylstyrene were added thereto over 30 minutes. The resultant solution was stirred at room temperature for 2 hours, and then 200 ml of chloroform were added thereto and dissolved. The solution was washed 3 times with water. The solvent was removed from the chloroform phase. The residue was purified by column chromatography to yield 11.6 g of p-vinylbenzylnaphthylamine as an intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509125B1
Source datasetuspto-grants-2003_01
ORD IDord-111a2351233e4c91b934c98ea48eb507
Source noteuspto-grants-2003_01