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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930163Generated: October 31, 2026

Methyl iodide → 2-(3,5-Difluoro-4-methoxyphenyl)propanoic acid

https://huagongshe.com/reaction/1930163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant(3,5-Difluoro-4-methoxyphenyl)acetic acidHCID 17750666—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-(3,5-Difluoro-4-methoxyphenyl)propanoic acidHCID 59627718105.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Lithium bis(trimethylsilyl)amide (25.4 mL, 25.35 mmol) was added to 2-(3,5-difluoro-4-methoxyphenyl)acetic acid (2.5 g, 12.37 mmol) in THF (60.8 mL) cooled to 0° C. under nitrogen. The resulting solution was stirred at 0° C. for 30 minutes. Next Methyl iodide (0.925 mL, 14.84 mmol) was added and the reaction stirred for 30 minutes Ammonium chloride (satd) (50 mL) added with vigorous stirring, ethyl acetate (100 mL) and water (50 mL) were added and the organic phase separated, washed with water (50 mL) and saturated brine (50 mL). The aq layer was acidified with 2M HCl (50 mL) and extracted with ethyl acetate. The organic layers were combined and dried over MgSO4, filtered and evaporated to afford 2-(3,5-difluoro-4-methoxyphenyl)propanoic acid (2.81 g, 105%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188092B2
Source datasetuspto-grants-2012_05
ORD IDord-62892c92bbb945c5b38d69800f6c3067
Source noteuspto-grants-2012_05