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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192646Generated: November 1, 2026

Methanol → Methyl 6-bromo-5-fluoropyridine-2-carboxylate

https://huagongshe.com/reaction/2192646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant6-Bromo-5-fluoropicolinic AcidHCID 53401194—
SolventEthyl AcetateHCID 8857—
ProductMethyl 6-bromo-5-fluoropyridine-2-carboxylateHCID 4631120499%

Reaction Steps

To a solution of 6-bromo-5-fluoropicolinic acid (1.0 equiv.) in methanol (0.2 M) was added H2SO4 (4.2 equiv.) and the reaction was stirred at room temperature for two hours. Upon completion of the reaction as monitored by LC/MS, the reaction was diluted with ethyl acetate and quenched slowly with saturated aqueous NaHCO3. The reaction was poured into a separatory funnel and extracted with ethyl acetate. The organic phase was dried with magnesium sulfate, filtered, and concentrated in vacuo to provide methyl 6-bromo-5-fluoropicolinate as a white solid (>99%). LC/MS=233.9/235.9 (M+H), Rt=0.69 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329732B2
Source datasetuspto-grants-2012_12
ORD IDord-8c5b856ce52140dabf175a01666bdb37
Source noteuspto-grants-2012_12