Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455549Generated: October 26, 2026

Acetic Acid → 5-Bromo-2-(4-iodophenoxy)nicotinic acid

https://huagongshe.com/reaction/455549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-IodophenolHCID 10894—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-2-chloronicotinic acidHCID 2763342—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Bromo-2-(4-iodophenoxy)nicotinic acidHCID 5747563786.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 3-neck 12 L flask equipped with an overhead stirrer, thermometer, condenser and nitrogen inlet was charged with NaH (186.1 g, 4.653 mol) and DMF (1500 mL). The slurry was cooled to 0° C. and a solution of 4-iodophenol (488.6 g, 2.221 mol) in DMF (1500 mL) and added. The temperature of the reaction mixture was maintained below 25-30° C. during this addition. After complete addition, the cooling bath was promptly removed and the mixture continued to stir at RT for 1 h. 5-Bromo-2-chloronicotinic acid (500 g, 2.115 mol) was then added to the slurry portion wise. The reaction mixture was heated to 115° C. overnight. The dark brown reaction mixture was cooled to 20° C. and diluted with water (2 L). The reaction mixture was acidified using HOAc (845 ml). The black homogenous solution (pH=5) was allowed to stir for 1 h at RT and poured slowly onto ice-water (20 L). The slurry was filtered at RT, washed with water (2×2 L) and dried in air to give 765 g of 5-Bromo-2-(4-iodophenoxy)-nicotinic acid as light orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497264B2
Source datasetuspto-grants-2013_07
ORD IDord-7fcb4d70242749e18f3b03597272f691
Source noteuspto-grants-2013_07