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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770907Generated: October 30, 2026

L-Methionine → 1-Bromo-3-fluoro-5-(methoxymethyl)benzene

https://huagongshe.com/reaction/1770907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-MethionineHCID 6137—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(3-Bromo-5-fluorophenyl)methanolHCID 2769402—
SolventEthyl AcetateHCID 8857—
Product1-Bromo-3-fluoro-5-(methoxymethyl)benzeneHCID 67979566231.1%

Reaction Steps

NaH (60% dispersion in mineral oil, 245 mg, 6.12 mmol) was added to a solution of (3-bromo-5-fluorophenyl)methanol (1.195 g, 5.83 mmol) in 2-Me THF (20 mL). After gas evolution had ceased, MeI (0.455 mL, 7.29 mmol) was added and the resulting mixture was stirred at r.t. for 16 h. Another portion of NaH (50 mg, 2.1 mmol) and Met (0.10 mL, 1.6 mmol) were added and the mixture was heated to 60° C. for 2 h. The cooled mixture was diluted with EtOAc, washed with water, dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography on silica (gradient of 0-15% EtOAc in heptane) to give 0.810 g (63% yield) of the title compound: 1H NMR (400 MHz, DMSO-d6) δ ppm 3.30 (s, 3H), 4.38-4.46 (m, 2H), 7.18 (m, 1H), 7.37 (s, 1H), 7.44-7.50 (m, 1H); MS (EI) m/z 218 M′.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248129B2
Source datasetuspto-grants-2016_02
ORD IDord-d72ee532f7da493d9a4cca6afd72c574
Source noteuspto-grants-2016_02