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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704639Generated: October 27, 2026

Methyl fluorosulfate → 2-Methyl-3-methoxy-1,2,5-thiadiazolium Fluorosulfonate

https://huagongshe.com/reaction/1704639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl fluorosulfateHCID 9870—
Reactant2-Methyl-1,2,5-thiadiazole-3-oneHCID 12495458—
SolventDichloromethaneHCID 6344—
Product2-Methyl-3-methoxy-1,2,5-thiadiazolium FluorosulfonateHCID 12495504—

Reaction Steps

2-Methyl-1,2,5-thiadiazole-3-one (11.6 g., 0.1 mole) was dissolved in dry methylene chloride (100 ml.) and under a nitrogen atmosphere was added methyl fluorosulfonate (8.2 ml., 0.1 mole) and the reaction mixture was stirred at room temperature for 1 hour. Further, methyl fluorosulfonate (0.1 ml.) was added and the reaction continued at reflux for one further hour. The reaction was cooled, the precipitate separated by filtration and washed with several portions of cold methylene chloride. Yield 13 g. The compound was stored in a dry atmosphere, m.p., 138°-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04127584
Source datasetuspto-grants-1978_11
ORD IDord-b005a1a1b05a492a9c356c16f9c9eb0a
Source noteuspto-grants-1978_11