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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427992Generated: October 29, 2026

Methyl iodide → Methyl 2-[2-(2,5-dimethylphenoxymethyl)phenyl]butyrate

https://huagongshe.com/reaction/427992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 18357786HCID 18357786—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductMethyl 2-[2-(2,5-dimethylphenoxymethyl)phenyl]butyrateHCID 1835779483%

Reaction Steps

A solution of 2-[2-(2,5-dimethylphenoxymethyl)phenyl]butyronitrile (0.67 g, 2.4 mmol) and 96% sodium hydroxide (0.73 g, 17.5 mmol) in ethanol (8 ml) was heated under reflux for 43 hours. The solvent was evaporated, and then water was added. The mixture was adjusted to pH 3 with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and then the solvent was evaporated. The crude product was dissolved in N,N-dimethylformamide (5 ml) and stirred at room temperature. Methyl iodide (0.50 g, 3.5 mmol) and potassium carbonate (0.50 g, 3.6 mmol) were added thereto in this order. After 1 hour, water was added, and the mixture was extracted with ethyl acetate. The extract was washed successively with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated, and the residue was purified by column chromatography on silica gel (n-hexane/ethyl acetate=9/1) to give the desired compound methyl 2-[2-(2,5-dimethylphenoxymethyl)phenyl]butyrate (0.62 g, 83%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313150B1
Source datasetuspto-grants-2001_11
ORD IDord-62b8a2a21d4a4c76b32620f9b47214a1
Source noteuspto-grants-2001_11