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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220557Generated: October 25, 2026

Methyl iodide → 1-(4-bromophenyl)ethyl methyl ether

https://huagongshe.com/reaction/220557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant1-(4-Bromophenyl)ethanolHCID 95352—
SolventDimethylformamideHCID 6228—
Product2-MethylpentaneHCID 7892—
Product1-(4-bromophenyl)ethyl methyl etherHCID 10965890195.2%

Reaction Steps

Dissolve 1-(4-bromo-phenyl)-ethanol (0.79 mL, 6.62 mmol) in dry N,N-dimethylformamide (7 mL) at ambient temperature under nitrogen atmosphere. Add sodium hydride (60% dispersion in oil, 397 mg, 9.93 mmol), stir the reaction for 30 min., then add methyl iodide (0.50 mL, 7.94 mmol) and stir the reaction for a further 23 hr. under nitrogen. Quench with water (30 mL), extract with DCM (3×30 mL), pass through an IST Phase Separator Frit® and concentrate. Purify using silica gel chromatography, eluting with 0:100 to 20:80 ethyl acetate: isohexane to give 1-bromo-4-(1-methoxy-ethyl)-benzene as a clear oil (1.39 g, 98%). 1H-NMR (400 MHz, CDCl3) δ 7.47 (d, 2H), 7.20 (d, 2H), 4.25 (q, 1H), 3.21 (s, 3H), 1.40 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-5f48e7b3fa16492d89c49e40f7742909
Source noteuspto-grants-2012_06