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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13274Generated: October 25, 2026

Sodium Carbonate → t-Butyl 2-(2-fluoro-5-nitro-phenyl)-pyrrole-1-carboxylate

https://huagongshe.com/reaction/13274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromo-1-fluoro-4-nitrobenzeneHCID 69699—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(tert-Butoxycarbonyl)-2-pyrroleboronic AcidHCID 2734321—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Productt-Butyl 2-(2-fluoro-5-nitro-phenyl)-pyrrole-1-carboxylateHCID 23145764—

Reaction Steps

1.1 g of tetrakis-triphenylphosphine palladium and 4.2 g of sodium carbonate were added to a solution of 4.3 g of 3-bromo-4-fluoro-nitrobenzene and 5.0 g of 1-(t-butoxycarbonyl)pyrrole-2-boronic acid in a mixture of 130 ml of dimethoxyethane and 22 ml of water, and the reaction liquid was heated overnight under reflux. Aqueous saturated sodium bicarbonate was added to the reaction liquid, and this was extracted with ethyl acetate. The organic layer was washed with water and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=20/1) to obtain the entitled compound as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728025B2
Source datasetuspto-grants-2010_06
ORD IDord-5b2c7caafde048c49c5bbc8275c188f1
Source noteuspto-grants-2010_06