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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131668Generated: November 2, 2026

Methyl iodide → N-(2-Methoxy-5-nitrobenzyl)acetamide

https://huagongshe.com/reaction/131668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 86760686HCID 86760686—
SolventAcetoneHCID 180—
ProductN-(2-Methoxy-5-nitrobenzyl)acetamideHCID 20650534—

Reaction Steps

N-(2-Methoxy-5-nitrobenzyl)acetamide 2-Acetamidomethyl-4-nitrophenol (2 g), sodium carbonate (2 g) and iodomethane (2 ml) were stirred in acetone (30 ml) at reflux 4 h. The mixture was filtered, the filtrate evaporated to dryness. The residue was warmed with aqueous sodium carbonate, washed with water and dried. Crystallised from ethanol/dilute acetic acid to give N-(2-methoxy-5-nitrobenzyl)acetamide as buff prisms. MP: 158.5-159.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384963B2
Source datasetuspto-grants-2008_06
ORD IDord-90d9c20ccdbb45d28f3a8b946592ef38
Source noteuspto-grants-2008_06