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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824737Generated: October 31, 2026

4-Toluenesulfonyl chloride → (4E)-5-(3-Pyridyl)-4-pentene-2-ol p-Toluenesulfonate

https://huagongshe.com/reaction/1824737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant(4E)-5-(3-Pyridyl)-4-penten-2-olHCID 12042974—
SolventPyridineHCID 1049—
Product(4E)-5-(3-Pyridyl)-4-pentene-2-ol p-ToluenesulfonateHCID 8746698760.1%

Reaction Steps

To a stirred solution of (4E)-5-(3-pyridyl)-4-penten-2-ol (5.00 g, 30.67 mmol) in dry pyridine (30 mL) at 0° C. was added p-toluenesulfonyl chloride (8.77 g, 46.01 mmol). The reaction mixture was stirred for 24 h at ambient temperature. The pyridine was removed by rotary evaporation. Toluene (50 mL) was added to the residue and subsequently removed by rotary evaporation. The crude product was stirred with a saturated solution of sodium bicarbonate (100 mL) and extracted with chloroform (3×100 mL). The combined chloroform extracts were dried over sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was purified by column chromatography over aluminum oxide, eluting with ethyl acetate-hexane (3:7, v/v). Selected fractions were combined and concentrated by rotary evaporation to give a viscous, brown oil (5.83 g, 60.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045538B2
Source datasetuspto-grants-2006_05
ORD IDord-ad3e8e8fc0ff4a01ae7f32a4f819a6d1
Source noteuspto-grants-2006_05