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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573105Generated: October 25, 2026

Dimethylformamide → Methyl 2-(5-bromopyridin-3-yloxy)-4-fluorobenzoate

https://huagongshe.com/reaction/573105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant3-Bromo-5-hydroxypyridineHCID 599529—
ReactantMethyl 2,4-DifluorobenzoateHCID 2782897—
ReactantPotassium tert-butoxideHCID 23665647—
Solvent2-MethyltetrahydrofuranHCID 7301—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-(5-bromopyridin-3-yloxy)-4-fluorobenzoateHCID 67227657—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of 5-bromopyridin-3-ol (1.060 g) in 2-methyltetrahydrofuran (15 mL) was added potassium tert-butoxide (6.09 mL, 1.0M in tetrahydrofuran) dropwise. After stirring for 5 minutes, methyl 2,4-difluorobenzoate (1.049 g) was added as a solution in 2-methyltetrahydrofuran (2 mL) and the reaction was heated to 75° C. N,N-Dimethylformamide (2 mL) was added to the reaction and the reaction was stirred overnight. The reaction was cooled, diluted with ethyl acetate (100 mL) and washed with water (50 mL), brine (50 mL), dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography (SF40-80) eluting with a gradient of 5% to 35% ethyl acetate/hexanes gave the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029404B2
Source datasetuspto-grants-2015_05
ORD IDord-4d177645839a45b0823d1cea560f7a46
Source noteuspto-grants-2015_05