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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175214Generated: November 3, 2026

Methyl iodide → Methyl 3-bromo-2-fluorobenzoate

https://huagongshe.com/reaction/1175214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl methyl etherHCID 15413—
Reactant3-Bromo-2-fluorobenzoic acidHCID 2736313—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-bromo-2-fluorobenzoateHCID 2158450589.5%

Reaction Steps

To a 100 mL round bottom flask was added 3-bromo-2-fluorobenzoic acid (5.00 g, 22.8 mmol, Oakwood), potassium carbonate (3.17 g, 22.9 mmol), and DMF (30 mL). Iodomethane, 2 M in MTBE (11.6 ml, 23.2 mmol) was added and the reaction mixture was stirred at RT for 16 hours. The reaction was filtered and the filtrate concentrated was in vacuo. The resulting brown crude residue was taken up with EtOAc and again filtered and concentrated to give methyl 3-bromo-2-fluorobenzoate (4.76 g, 20.4 mmol, 89.5% yield), as a brown syrup that was used in the Step 2 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838676B2
Source datasetuspto-grants-2010_11
ORD IDord-6f3bda2a993f464c88614095c260e517
Source noteuspto-grants-2010_11