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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065133Generated: October 25, 2026

Octyl triflate → 2-Octyl-3,4,5-trichloroisothiazolium trifluoromethane sulfonate

https://huagongshe.com/reaction/1065133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctyl triflateHCID 10869071—
ReactantTrichloroisothiazoleHCID 12333154—
SolventDiethyl EtherHCID 3283—
Product2-Octyl-3,4,5-trichloroisothiazolium trifluoromethane sulfonateHCID 1453570931%

Reaction Steps

Trichloroisothiazole (6.6 g, 0.035 mol) and n-octyl trifluoromethane sulfonate (7.5 g, 0.0286 ml) were heated at 110° for 2 hrs. After cooling, 150 ml of ether was added and solution cooled in a dry ice/acetone bath. The ether was decanted and the brown oil dried to yield 4.0 g (31%) of product. Spectral data (NMR and IR) were consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04328347
Source datasetuspto-grants-1982_05
ORD IDord-d55342daf06f44509d256b92f43648af
Source noteuspto-grants-1982_05