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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741382Generated: October 31, 2026

p-Toluenesulfonic acid → 1-(4,5-Diphenyloxazol-2-yl)-8-(3-methoxybenzyl)-1-cyclooctene

https://huagongshe.com/reaction/1741382

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1-(Hydroxy)-1-(4,5-diphenyloxazol-2-yl)-2-(3-methoxybenzyl)cyclooctaneHCID 18367289—
SolventTolueneHCID 1140—
Product1-(4,5-Diphenyloxazol-2-yl)-8-(3-methoxybenzyl)-1-cycloocteneHCID 54307632112.9%

Reaction Steps

A mixture of 1-(hydroxy)-1-(4,5-diphenyloxazol-2-yl)-2-(3-methoxybenzyl)cyclooctane (3.5 g) and p-toluenesulfonic acid (500 mg) in toluene (50 ml) was stirred for 4 hours under reflux. The solution was washed with water, sat. NaHCO3, and brine, dried over MgSO4, and evaporated in vacuo. The residue was purified by chromatography on silica gel to afford 1-(4,5-diphenyloxazol-2-yl)-8-(3-methoxybenzyl)-1-cyclooctene (3.8 g). MS (m/z): 450 (M+ +1) IR (Neat): 1600 cm-1NMR (CDCl3, δ): 1.4-2.0.(8H, m), 2.2-2.4 (2H, m), 3.0 (1H, m), 3.2-3.5 (2H, m), 3.78 (3H, s), 6.65 (1H, s), 6.7-7.0 (3H, m), 7.18 (1H, t, J=8 Hz), 7.2-7.8 (11H, m)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972965
Source datasetuspto-grants-1999_10
ORD IDord-1b379c2cfd1448db96ba99d89df9bdd8
Source noteuspto-grants-1999_10