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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611600Generated: October 26, 2026

Bromobenzene → 3-Phenyl-2-thiophenecarboxaldehyde

https://huagongshe.com/reaction/1611600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantSodium CarbonateHCID 10340—
Reactant2-Formyl-3-thiopheneboronic acidHCID 2773426—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
Product3-Phenyl-2-thiophenecarboxaldehydeHCID 81884753.6%

Reaction Steps

2-Formylthiophen-3-boronic acid (4) (0.89 g, 5.7 mmol) dissolved in 96% ethanol (15 ml) was added dropwise to a mixture of 2-bromobenzene (0.66 ml, 6.2 mmol) in benzene (12 ml), (Ph3P)4Pd (197 mg, 0.15 mmol) and an aqueous solution of 2M Na2CO3 (6.3 ml). The reaction mixture was then refluxed for 6 hrs. Then the mixture was cooled to room temperature, the solvent was partially removed under reduced pressure and the resulting mixture was extracted with ethyl ether (4×100 ml). The combined organic layer was washed with a saturated solution of NaCl, dried (Na2SO4), and evaporated under reduced pressure. The mixture was chromatographed using 95/5 petroleum ether/ethyl acetate, thus giving the derivative (5) (0.575 g, [lacuna] mmol, 53% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06989388B2
Source datasetuspto-grants-2006_01
ORD IDord-90c1d3a23dac4e159f01f017b72d68fa
Source noteuspto-grants-2006_01