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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827282Generated: October 31, 2026

Sodium Carbonate → 2-(Thiophen-2-yl)benzaldehyde

https://huagongshe.com/reaction/1827282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-BromobenzaldehydeHCID 81129—
Reactant2-Thiopheneboronic acidHCID 2733960—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(Thiophen-2-yl)benzaldehydeHCID 2795558—

Reaction Steps

To a mixture of 2-bromobenzaldehyde (1.17 mL, 10.0 mmol) and 2.0 M aqueous sodium carbonate (75 mL) in DME (225 mL) were added thiophene-2-boronic acid (1.53 g, 12.0 mmol) and tetrakis(triphenylphosphine)palladium[0] (578 mg, 0.5 mmol). The mixture was heated to reflux under nitrogen for 16 hr. The resulting solution was cooled, and the crude product was extracted from aqueous solution with ethyl acetate. The organic layer was dried over MgSO4, and the solvents were removed under vacuum. The crude product was purified on flash column with 25% DCM in hexane to yield 2-(2-thienyl)benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053101B2
Source datasetuspto-grants-2006_05
ORD IDord-e31b7258edea4f77b422fef3a43d7df5
Source noteuspto-grants-2006_05