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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298353Generated: October 31, 2026

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

https://huagongshe.com/reaction/2298353

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 vacua. 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 (6.2g, 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 numberUS06492385B2
Source datasetuspto-grants-2002_12
ORD IDord-8182313c75714ab08066be1f56056b1f
Source noteuspto-grants-2002_12