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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15061Generated: October 25, 2026

Chloromethyl Methyl Ether → 4-Fluoro-3-(methoxymethoxy)benzyl alcohol

https://huagongshe.com/reaction/15061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant4-Fluoro-3-hydroxybenzoic acidHCID 593635—
SolventEthyl AcetateHCID 8857—
Product4-Fluoro-3-(methoxymethoxy)benzyl alcoholHCID 2307431194%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (1.07 mL) and methoxymethyl chloride (2.24 mL) were added to tetrahydrofuran (10 mL) solution of 4-fluoro-3-hydroxybenzoic acid (1.0 g), and stirred at 0° C. for 2 hours. Ethyl acetate was added to the reaction liquid which then was washed with water and saturated brine, dried over anhydrous magnesium sulfate, the solvent therein was concentrated under reduced pressure and the residue was dissolved in tetrahydrofuran (20 mL). Lithiumaluminium hydride (360 mg) was added, stirred at 0° C. for an hour, ethyl acetate was added and the insoluble matter was removed, followed by washing with saturated brine and drying over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, the title compound (1.14 g, 94%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732456B2
Source datasetuspto-grants-2010_06
ORD IDord-b32e232e6caf496cb7414acd838cedd1
Source noteuspto-grants-2010_06