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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267332Generated: October 30, 2026

4-Toluenesulfonyl chloride → 2-Tosylthiophene

https://huagongshe.com/reaction/2267332

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantThiopheneHCID 8030—
CatalystZincchlorideHCID 3007855—
SolventAcetonitrileHCID 6342—
Product2-TosylthiopheneHCID 25552195.5%

Reaction Steps

A mixture of p-toluenesulfonyl chloride (3 g, 15.7 mmol) and zinc chloride (3 g, 21.3 mmol) in acetonitrile (30 mL) was heated to reflux and thiophene (2.4 g, 28.5 mmol) was added dropwise. After refluxing for 4 h the mixture was cooled to rt and filtered through Celite. The filtrate was concentrated in vacuo and then 100 mL of sodium hydroxide (2 N) was added. The mixture was extracted with ethyl acetate (3×60 mL) and the combined organic layers were washed with hydrochloric acid (10%, 50 mL) and brine (100 mL), dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated in vacuo and the product was purified by flash chromatography eluting with dichloromethane/hexane (2:3) to give the title compound (0.54 g, 15 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-dcd43305a0ed45b6af4702663bdb4623
Source noteuspto-grants-2010_12