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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | p-Vinylbenzyl chloride | HCID 74126 | — |
| Reactant | 1-Pentylnaphthalene | HCID 518732 | — |
| Catalyst | 2,5-Di-tert-butylhydroquinone | HCID 2374 | — |
| Catalyst | Sodium Iodide | HCID 5238 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 59620855 | HCID 59620855 | 77.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06509125B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-111a2351233e4c91b934c98ea48eb507 |
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| Source note | uspto-grants-2003_01 |
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