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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892261Generated: October 30, 2026

m-Chloroperbenzoic acid → 1-[2-(2-Methyl-4-{2-[2-(E)-(4-trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenylmethanesulfonyl)-ethyl]-1H-[1,2,3]triazole

https://huagongshe.com/reaction/892261

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant1-[2-(2-Methyl-4-{2-[2-(e)-(4-trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl-methanesulfinyl)-ethyl]-1h[1,2,3]triazoleHCID 22242068—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1-[2-(2-Methyl-4-{2-[2-(E)-(4-trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenylmethanesulfonyl)-ethyl]-1H-[1,2,3]triazoleHCID 1154123353%

Reaction Steps

35 mg (0.15 mmol) 75% 3-chloroperoxybenzoic acid dissolved in 5 ml ethyl acetate were given at −30° C. to solution of 52 mg (0.10 mmol) 1-[2-(2-methyl-4-{2-[2-(E)-(4-trifluoromethoxy-phenyl)-vinyl]-oxazol-4-ylmethoxy}-phenyl-methanesulfinyl)-ethyl]-1H[1,2,3]triazole in 25 ml dichloromethane. The mixture was stirred for 48 h and slowly allowed to reach room temperature. Additional 20 ml dichloromethane were added, washed with conc. sodium carbonate solution, water, dried and evaporated to give 29 mg (53%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07005526B2
Source datasetuspto-grants-2006_02
ORD IDord-5b36142630494e9a80413d7938df399d
Source noteuspto-grants-2006_02