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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282240Generated: October 26, 2026

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

https://huagongshe.com/reaction/1282240

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 numberUS06455554B1
Source datasetuspto-grants-2002_09
ORD IDord-2720ee4c4c7b427abb67752a93ad1b58
Source noteuspto-grants-2002_09