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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915899Generated: October 31, 2026

(E)-2,3-dibromo-4-oxobut-2-enoic acid → 5-Bromo-2-(2-fluorophenyl)pyrimidine-4-carboxylic acid

https://huagongshe.com/reaction/1915899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-2,3-dibromo-4-oxobut-2-enoic acidHCID 2723705—
ReactantSodium ethoxideHCID 2723922—
Reactant2-FluorobenzamidineHCID 4323059—
SolventEthanolHCID 702—
Product5-Bromo-2-(2-fluorophenyl)pyrimidine-4-carboxylic acidHCID 82168673—

Reaction Steps

Sodium ethoxide (21 mass % in ethanol; 8.69 mL, 23.268 mmol) was added to an ice-bath cooled mixture of 2-fluorobenzamidine (2.71 g, 15.512 mmol) in ethanol (100 mL). The resulting mixture was allowed to warm to room temperature and stirred at rt (room temperature) under nitrogen for 30 min. To the reaction mixture was added a solution of (E)-2,3-dibromo-4-oxo-but-2-enoic acid (2.00 g, 7.7561 mmol) in ethanol (20 ml). The mixture was heated at 50° C. for 3 h. After cooling to RT, the reaction was concentrated in vacuo. Water and 1M NaOH (˜50 ml) were added and the aqueous mixture was extracted with EtOAc. The aqueous phase was acidified to pH4 with 1N HCl (about 30 ml), then extracted with EtOAc 3×. Combined organic extracts were dried over sodium sulfate, filtered and concentrated to gave 5-bromo-2-(2-fluorophenyl)pyrimidine-4-carboxylic acid, 770 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614206B2
Source datasetuspto-grants-2013_12
ORD IDord-f66b542cb56249499a1599913708a013
Source noteuspto-grants-2013_12