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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384406Generated: October 29, 2026

Sodium Carbonate → HCID 57483854, compound

https://huagongshe.com/reaction/384406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 5-bromofuran-2-carboxylateHCID 599633—
Reactant2-(2-Methoxy-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 57483800—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57483854HCID 5748385418%

Reaction Steps

2-(2-Methoxy-3-nitro-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 6a (3.6 g, 12 mmol), 5-bromofuran-2-carboxylic acid methyl ester (2.05 g, 10 mmol), tetrakis(triphenylphosphine)palladium (1.55 g, 0.5 mmol) and sodium carbonate (2.12 g, 20 mmol) were dissolved in 1,4-dioxane. The reaction mixture was heated to reflux for 3 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was diluted with 30 mL of water and 50 mL of ethyl acetate. The separated organic layer was concentrated under reduced pressure and recrystallized from a solvent mixture of ethyl acetate and n-hexane to obtain the title compound 5-(2-methoxy-3-nitro-phenyl)-furan-2-carboxylic acid methyl ester 54a (500 mg, yield 18%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-0ea3d7d4141f47c2a4c59efef0929f4f
Source noteuspto-grants-2013_02