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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272513Generated: October 29, 2026

Methyl iodide → Methyl 6-bromopyridine-2-carboxylate

https://huagongshe.com/reaction/1272513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Bromopyridine-2-carboxylic acidHCID 593919—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 6-bromopyridine-2-carboxylateHCID 16217886—

Reaction Steps

Treat 6-bromopicolinic acid (1.99 g) in DMF (10 mL) with potassium carbonate (1.40 g) and then methyl iodide (4 mL) at room temperature for 20 h. Dilute the reaction mixture with dichloromethane (60 mL) and filter. Extract the filtrate with brine (twice), dry (MgSO4), and concentrate in vacuo to give methyl 6-Bromopicolinate pale yellow solid (1.75 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208602B2
Source datasetuspto-grants-2007_04
ORD IDord-02f9b0d8750b422cb3820e924d6e426a
Source noteuspto-grants-2007_04