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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853765Generated: October 30, 2026

Methyl iodide → Methyl 6-bromopyridine-2-carboxylate

https://huagongshe.com/reaction/853765

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 1621788682.2%

Reaction Steps

6-bromopicolinic acid (1.99 g) in DMF (10 mL) was treated with potassium carbonate (1.40 g) and then methyl iodide (4 mL) at room temperature for 20 h. The reaction mixture was diluted with dichloromethane (60 mL) and filtered. The filtrate was extracted with brine (twice), dried (MgSO4), and concentrated under vacuum to give methyl 6-bromopicolinate as a pale yellow solid (1.75 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256186B2
Source datasetuspto-grants-2007_08
ORD IDord-ceb6d0b498cc4bc49efc07039e6520c3
Source noteuspto-grants-2007_08