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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301861Generated: November 4, 2026

p-Chlorothiophenol → 5-[(4-Chlorophenyl)sulfanyl]-2-thiophenecarbaldehyde

https://huagongshe.com/reaction/2301861

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ChlorothiophenolHCID 7815—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromothiophene-2-carbaldehydeHCID 78428—
SolventTetrahydrofuranHCID 8028—
Product5-[(4-Chlorophenyl)sulfanyl]-2-thiophenecarbaldehydeHCID 706219498%

Reaction Steps

Sodium hydride (60%, 1.2 g, 30 mmol) is added to a solution of 4-chlorothiophenol (4.3 g, 30 mmol) in THF (30 mL). The resulting solution is stirred for 10 minutes then the solvent is removed in vacuo. Acetone (60 mL) is added followed by 5-bromothiophene-2-carboxaldehyde (3.0 mL, 25 mmol). The mixture is stirred at room temperature for 2 hours. The solvent is removed in vacuo and the resulting slurry diluted with CH2Cl2. This solution is washed three times with 1N NaOH then dried over MgSO4, filtered and concentrated in vacuo. The crude product is purified by flash column chromatography (gradient of 1 to 5% EtOAc in heptane) to give the desired product (6.2 g, 98%). 1H NMR (300 MHz, CDCl3) δ 7.13, 7.31-7.39, 7.63, 9.78.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500840B2
Source datasetuspto-grants-2002_12
ORD IDord-d5f5e306526a434297fe363d4730d719
Source noteuspto-grants-2002_12