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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878759Generated: October 26, 2026

Methyl iodide → [4-(2-Methoxyethoxy)phenyl]methanol

https://huagongshe.com/reaction/878759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantLithium borohydrideHCID 4148881—
Reactant4-(2-Methoxyethoxy)benzoic acidHCID 6485562—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product[4-(2-Methoxyethoxy)phenyl]methanolHCID 1202297168%

Reaction Steps

To a solution of 4-(2-methoxyethoxy)benzoic acid (100 mg, 0.51 mmol) in N,N-dimethylformamide (2 mL) were added potassium carbonate (282 mg, 2.04 mmol) and iodomethane (79 μL, 1.27 mmol) at room temperature. The mixture was stirred at the same temperature overnight, and then to the reaction solution was added water. The mixture was extracted with ethyl acetate twice. The organic layer was combined, washed with water and saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was dissolved in tetrahydrofuran (3 mL), and then thereto was added lithium borohydride (53 mg, 2.45 mmol) at 0° C. The reaction solution was slowly warmed to room temperature, and stirred for 3 days. To the reaction solution was added water, and the mixture was extracted with ethyl acetate twice. The organic layer was combined, washed with water and saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to give [4-(2-methoxyethoxy)phenyl]methanol (61 mg, 68%) as a colorless and clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987445B2
Source datasetuspto-grants-2015_03
ORD IDord-13cbe3c0e7974beaa3c8308f772b6b6e
Source noteuspto-grants-2015_03