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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836678Generated: November 4, 2026

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

https://huagongshe.com/reaction/1836678

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 numberUS06777421B2
Source datasetuspto-grants-2004_08
ORD IDord-f864db07518b4978bae3c45030eddb1c
Source noteuspto-grants-2004_08