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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711518Generated: October 26, 2026

4-Toluenesulfonyl chloride → HCID 87466225, compound

https://huagongshe.com/reaction/1711518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant(2S)-(4E)-5-(5-Isopropoxy-3-pyridyl)-4-penten-2-olHCID 68477280—
SolventTriethylamineHCID 8471—
ProductHCID 87466225HCID 87466225—

Reaction Steps

Under a nitrogen atmosphere, p-toluenesulfonyl chloride (11.45 g, 60.06 mmol) was added to a stirring solution of (2S)-(4E)-5-(5-isopropoxy-3-pyridyl)-4-penten-2-ol (7.00 g, 31.63 mmol) in dry triethylamine (30 mL) at 0° C. After stirring and warming to ambient temperature over 18 h, the mixture was concentrated on a rotary evaporator. The crude product was stirred with saturated NaHCO3 solution (100 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 10.00 g (84.2%) as a dark-brown oil, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790757B2
Source datasetuspto-grants-2010_09
ORD IDord-c0d9e37ab4aa46e692bd43a334e160f3
Source noteuspto-grants-2010_09