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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394153Generated: November 1, 2026

Sodium Carbonate → 5-[2-(Trifluoromethoxy)phenyl]-2-thiophenecarboxaldehyde

https://huagongshe.com/reaction/1394153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant5-Formyl-2-thiopheneboronic acidHCID 2773430—
Reactant1-Bromo-2-(trifluoromethoxy)benzeneHCID 2777266—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
Product5-[2-(Trifluoromethoxy)phenyl]-2-thiophenecarboxaldehydeHCID 16768678—

Reaction Steps

To a solution of 2-trifluoromethoxy-1-bromobenzene (0.21 mL) and 5-formyl-2-thiophene boronic acid (0.23 g) in DME (11 mL) were added Pd(OAc)2 (0.014 g) and Ph3P (0.033 g) followed by 2M sodium carbonate (1 mL) and water (1 mL). The mixture was stirred at rt for 3 h. The reaction was diluted with ethylacetate (20 mL) and washed with water and brine, and then dried (sodium sulfate). The crude product was purified by flash-chromatography using acetone-hexanes (1:4) to give the desired 5-(2-trifluoromethoxyphenyl)thiophene-2-aldehyde as an oil [MS data: m/e 273 (M+1)+]. The aldehyde (0.15 g), thus obtained, was then condensed with 2,4-thiazolidine-2,4-dione in the presence of benzoic acid and piperidine under the conditions described in EXAMPLE 5 to give the title compound 5-(5-(2-trifluoromethoxyphenyl)thienylidene)thiazolidine-2,4-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348348B2
Source datasetuspto-grants-2008_03
ORD IDord-83e75f9df52e4f699f967937269e0883
Source noteuspto-grants-2008_03