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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677254Generated: October 27, 2026

Methyl iodide → 2-(5-Chloro-2-isopropyl-4-methoxy-phenoxy)-3-methoxy-acrylonitrile

https://huagongshe.com/reaction/1677254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl formateHCID 8025—
ReactantSodium hydrideHCID 24758—
Reactant(5-Chloro-2-isopropyl-4-methoxy-phenoxy)-acetonitrileHCID 59598662—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(5-Chloro-2-isopropyl-4-methoxy-phenoxy)-3-methoxy-acrylonitrileHCID 6705342284%

Reaction Steps

To a solution of (5-chloro-2-isopropyl-4-methoxy-phenoxy)-acetonitrile (1.44 g, 6.0 mmol) and ethyl formate (2.2 g, 29.2 mmol) in 7 mL 1,2-dimethoxy ethane at 5° C. was added 95% NaH (0.15 g, 6.0 mmol) in one portion. The mixture was warmed to room temperature. After 1 hour 95% NaH (0.15 g, 6.0 mmol) was added in one portion. After 1 hour 10 mL iodomethane was added and the mixture was allowed to stir for 16 hour. The mixture was concentrated in vacuo, 1N HCl was added and the mixture was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. Purification via flash chromatography (85:15 hexane/ethyl acetate) afforded 2-(5-chloro-2-isopropyl-4-methoxy-phenoxy)-3-methoxy-acrylonitrile (1.41 g, 84%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008313B2
Source datasetuspto-grants-2011_08
ORD IDord-72fb7d0cc24043b8afaa3ef7de3e567f
Source noteuspto-grants-2011_08