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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25125Generated: October 30, 2026

Pyridine → 4-(4-Methoxyphenyl)butyl 4-methylbenzene-1-sulfonate

https://huagongshe.com/reaction/25125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant4-(4-Methoxyphenyl)butan-1-olHCID 97660—
SolventChloroformHCID 6212—
Product4-(4-Methoxyphenyl)butyl 4-methylbenzene-1-sulfonateHCID 1104590170.1%

Reaction Steps

Pyridine (15 mL) was added drop wise to a cooled (0° C.) solution of 4-(4-methoxyphenyl)butanol (10.0 g, 0.055 mol) and p-toluenesulfonyl chloride (13.6 g, 0.072 mol) in dry chloroform (100 mL) under stirring. The reaction mixture was stirred overnight at room temperature. After this time, the reaction was quenched with 10% HCl (300 mL) and extracted with chloroform. The organic fraction was washed with saturated NaHCO3, water and dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue purified by flash chromatography (eluent:hexane/ethyl acetate 15:1) to provide 12.9 g (66%) of 1 as clear oil. 1H NMR (360 MHz, CDCl3) δ 1.61 (m, 4H), 2.44 (s, 3H), 2.52 (m, 2H), 3.78 (s, 3H), 4.05 (m, 2H), 6.77 (d, 2H), 7.05 (d, 2H), 7.34 (d, 2H), 7.78 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858615B2
Source datasetuspto-grants-2005_02
ORD IDord-a58961e48bd74daebc9cb4543b0c51f4
Source noteuspto-grants-2005_02