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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513006Generated: November 3, 2026

Sodium Iodide → 2,3-Difluoro-6-[2-(methoxymethyloxy)ethoxy]benzaldehyde

https://huagongshe.com/reaction/1513006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-2-(methoxymethoxy)ethaneHCID 3331051—
Reactant2,3-Difluoro-6-hydroxybenzaldehydeHCID 21221031—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2,3-Difluoro-6-[2-(methoxymethyloxy)ethoxy]benzaldehydeHCID 86641276—

Reaction Steps

A mixture of 2,3-difluoro-6-hydroxybenzaldehyde (2.17 g), 2-(methoxymethyloxy)-ethyl bromide (1.92 mL), potassium carbonate (2.85 g) and sodium iodide (0.41 g) in N,N-dimethylformamide (20 mL) was stirred at room temperature overnight. The reaction mixture was poured into water, and the resulting mixture was extracted with diethyl ether. The extract was washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=4/1-1/1) to give 2,3-difluoro-6-[2-(methoxymethyloxy)ethoxy]benzaldehyde (1.02 g). This material was dissolved in tetrahydrofuran (15 mL). To the solution were added water (1.5 mL) and sodium borohydride (92 mg), and the mixture was stirred at room temperature for 1 hour. The reaction mixture was poured into 10% aqueous sodium chloride solution, and the resulting mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure to give the title compound (1.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217069B2
Source datasetuspto-grants-2012_07
ORD IDord-f67b5df5497f48afb0cd23a05aaad372
Source noteuspto-grants-2012_07