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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977601Generated: October 31, 2026

Methyl iodide → 3-(3-cyclopentyloxy-4-methoxy-N-methylanilino)-2-cyclopenten-1-one

https://huagongshe.com/reaction/1977601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant3-(3-Cyclopentyloxy-4-methoxyanilino)-2-cyclopenten-1-oneHCID 15521354—
SolventDimethylformamideHCID 6228—
Product3-(3-cyclopentyloxy-4-methoxy-N-methylanilino)-2-cyclopenten-1-oneHCID 994419094.8%

Reaction Steps

0.10 g (0.35 mmole) of 3-(3-cyclopentyloxy-4-methoxyanilino)-2-cyclopenten-1-one produced in Example 1, 0.02 g of sodium hydride (60%), and 0.06 g (0.42 mmole) of methyl iodide were dissolved in 4 ml of N,N-dimethylformamide and the solution was stirred at room temperature for one night. The reaction solution was quenched with water, then was extracted with methylene chloride. The extract was dried over anhydrous magnesium sulfate, and the solvent was removed in vacuo to obtain a crude product. The crude product was purified by flash chromatography (SiO2; eluted by 2% methanol/methylene chloride) to obtain the title compound 0.10 g (yield 93.4%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235736B1
Source datasetuspto-grants-2001_05
ORD IDord-3aba3563d5884ff3ad3519827a91a041
Source noteuspto-grants-2001_05