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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711505Generated: October 26, 2026

4-Toluenesulfonyl chloride → (2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonate

https://huagongshe.com/reaction/1711505

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium BicarbonateHCID 516892—
Reactant(2S)-(4E)-5-(3-Pyridyl)-4-penten-2-olHCID 20655737—
SolventTriethylamineHCID 8471—
Product(2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonateHCID 8746599468.6%

Reaction Steps

Under a nitrogen atmosphere, p-toluenesulfonyl chloride (7.01 g, 36.77 mmol) was added to a stirring solution of (2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol (3.00 g, 18.38 mmol) in dry triethylamine (20 mL) at 0° C. After stirring and warning to ambient temperature over 18 h, the mixture was stirred with cold, saturated NaHCO3 solution (50 mL) for 1 hour and extracted with chloroform (3×50 mL). The combined chloroform extracts were dried (K2CO3), filtered, and concentrated by rotary evaporation to afford a thick, dark-brown mass (˜7 g). The crude product was purified by column chromatography on silica gel, eluting with chloroform-acetone (98:2, v/v) to afford 4.00 g (68.6%) of a light-brown syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790757B2
Source datasetuspto-grants-2010_09
ORD IDord-31d6d19e69274736a64ad8b256a2e8fe
Source noteuspto-grants-2010_09