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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065134Generated: October 26, 2026

2-Propen-1-yl 1,1,1-trifluoromethanesulfonate → 2-(2-Propen-1-yl)-3,4,5-trichloroisothiazolium trifluoromethane sulfonate

https://huagongshe.com/reaction/1065134

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Propen-1-yl 1,1,1-trifluoromethanesulfonateHCID 10932223—
ReactantTrichloroisothiazoleHCID 12333154—
SolventCarbon TetrachlorideHCID 5943—
Product2-(2-Propen-1-yl)-3,4,5-trichloroisothiazolium trifluoromethane sulfonateHCID 1309718330%

Reaction Steps

Trichloroisothiazole (5.7 g, 0.03 ml) and a solution of allyl trifluoromethane sulfonate (0.03 mol) in CCl4 were heated and excess CCl4 was removed by distillation until the reacting temperature reached 90° C. After heating at 90° for 30 min, the reaction was cooled and 150 ml of ether added. The solid was collected to yield 2.6 g (30%) of product, mp 103-105. 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-facd532933f84d1c981d974f97b0cf05
Source noteuspto-grants-1982_05