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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331045Generated: October 26, 2026

Chloromethyl Methyl Ether → 4-Bromo-1-fluoro-2-(methoxymethoxy)benzene

https://huagongshe.com/reaction/331045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
ReactantPhenol, 5-bromo-2-fluoro-HCID 183421—
SolventDimethylformamideHCID 6228—
Product4-Bromo-1-fluoro-2-(methoxymethoxy)benzeneHCID 6686605395.8%

Reaction Steps

To a stirred solution of 5-bromo-2-fluorophenol (5 g, 26.2 mmol) in DMF (50 mL) at 0° C. was added sodium hydride (1.571 g, 39.3 mmol). After stirring for 10 min, chloromethyl methyl ether (2.386 mL, 31.4 mmol) was added dropwise to mixture and the mixture was then stirred for 1 hour at 0° C. The reaction was quenched with addition of saturated NH4Cl aq. and the mixture was poured into water (150 mL). The mixture was extracted with ethyl acetate (30 mL×2). The organic layers were combined, washed with brine (100 mL), dried over MgSO4, filtered and evaporated in vacuo. The crude residue was purified by chromatography on silica, eluting with a gradient of 0-10% ethyl acetate in cyclohexane to give the title compound (5.90 g). 1H NMR (CDCl3, 400 MHz) δ ppm: 3.55 (3H, s), 5.24 (2H, s), 6.95-7.02 (1H, m), 7.08-7.14 (1H, m), 7.36-7.40 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877742B2
Source datasetuspto-grants-2014_11
ORD IDord-1c7eb7f648964c12ae5294fb4e420c08
Source noteuspto-grants-2014_11