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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Bromo-1-fluoro-4-nitrobenzene | HCID 69699 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(tert-Butoxycarbonyl)-2-pyrroleboronic Acid | HCID 2734321 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | t-Butyl 2-(2-fluoro-5-nitro-phenyl)-pyrrole-1-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728025B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-5b2c7caafde048c49c5bbc8275c188f1 |
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| Source note | uspto-grants-2010_06 |
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