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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414253Generated: November 1, 2026

Methyl iodide → 2-[4-Chloro-3-(methoxycarbonylaminomethyl)phenyl]-2-methoxyiminoacetonitrile

https://huagongshe.com/reaction/2414253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-[4-Chloro-3-(methoxycarbonylaminomethyl)phenyl]-2-hydroxyiminoacetonitrileHCID 86759549—
SolventMethanolHCID 887—
Product2-[4-Chloro-3-(methoxycarbonylaminomethyl)phenyl]-2-methoxyiminoacetonitrileHCID 8675955047.5%

Reaction Steps

0.36 g of 2-[4-chloro-3-(methoxycarbonylaminomethyl)phenyl]-2-hydroxyiminoacetonitrile and 0.54 g of a 28% sodium methylate methanol solution were added to 5 ml of methanol, and 0.49 g of methyl iodide was added thereto, followed by stirring at room temperature for 24 hours. The reaction solution was vacuum concentrated, the solvent was distilled off, water was added to the residue, extraction with ethyl acetate was carried out, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (Wakogel C-200, eluent: hexane/ethyl acetate=4/1-5/1) to obtain 0.18 g of 2-[4-chloro-3-(methoxycarbonylaminomethyl)phenyl]-2-methoxyiminoacetonitrile as colorless crystals (m.p. 104-107° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06812229B1
Source datasetuspto-grants-2004_11
ORD IDord-1707d261c467416fb1b0d704048b667a
Source noteuspto-grants-2004_11