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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271401Generated: November 1, 2026

p-Toluenesulfonic acid → 1-[4-(4-{2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-butyl]-1H-[1,2,3]triazolium p-toluenesulfonate

https://huagongshe.com/reaction/1271401

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1-[4-(4-{2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-butyl]-1H-[1,2,3]triazoleHCID 69474406—
SolventEthanolHCID 702—
Product1-[4-(4-{2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-butyl]-1H-[1,2,3]triazolium p-toluenesulfonateHCID 86594702—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 0.124 g (0.26 mmol) 1-[4-(4-{2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-butyl]-1H-[1,2,3]triazole in 20 ml EtOH 0.973 μl (50 mg/ml in EtOH) of p-toluenesulfonic acid was added and heated to 60° C. for complete dissolution. After evaporation of the solvent the oily residue crystallized slowly to yield 1-[4-(4-{2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl)-butyl]-1H-[1,2,3]triazolium p-toluenesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205325B2
Source datasetuspto-grants-2007_04
ORD IDord-f96dcf38ae1343d29c0f1f41f7bb0205
Source noteuspto-grants-2007_04