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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705230Generated: October 27, 2026

Sodium ethoxide → 5-Bromo-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid

https://huagongshe.com/reaction/705230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantMucobromic AcidHCID 3033972—
Reactant2,6-Difluorobenzamidine hydrochlorideHCID 46318424—
SolventEthanolHCID 702—
Product5-Bromo-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acidHCID 66652334—

Reaction Steps

A 2.68 M NaOEt in EtOH solution (3 eq) was added to an ice-bath cooled mixture of 2,6-difluorobenzimidamide hydrochloride (2 eq) in EtOH (0.1 M). The resulting mixture was allowed to warm to rt and stirred under N2 for 30 min. To the reaction mixture was added drop wise a solution of mucobromic acid (1 eq) in EtOH and the reaction was heated in a 50° C. oil bath for 2.5 hr. After cooling to rt the reaction mixture was concentrated in vacuo. H2O and 1.0 N NaOH were added and the aqueous mixture was washed with EtOAc. The aqueous phase was acidified to pH=4 with 1.0 N HCl then extracted with EtOAc. Combined organic extracts were washed once with brine, then dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to give 5-bromo-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid. The crude product was used for the next step without further purification. LC/MS (m/z): 316.9 (MH+). LC: Rt: 2.426 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173883B2
Source datasetuspto-grants-2015_11
ORD IDord-cc58828662804ddfa8013d3f5842eb3e
Source noteuspto-grants-2015_11