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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742058Generated: November 4, 2026

Acetonitrile → 3,5-Dichloro-1-fluoropyridinium triflate

https://huagongshe.com/reaction/1742058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant3,5-DichloropyridineHCID 17153—
ReactantTrifluoromethanesulfonic acidHCID 62406—
SolventPyridineHCID 1049—
Product3,5-Dichloro-1-fluoropyridinium triflateHCID 2724578180.7%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To 40 ml of acetonitrile were added 3.087 g (20.860 mmol ) of 3,5-dichloropyridine and 3.039 g (20.250 mmol ) of trifluoromethanesulfonic acid (i.e., the amount pyridine compound was 1.03 times that of trifluoromethanesulfonic acid in a molar ratio), and the mixture was cooled to -20° C. The following procedures were conducted as in Example 1, and 5.774 g (18.3 mmol) of N-fluoro-3, 5-dichloropyridinium trifluoromethanesulfonate were obtained with a yield of 90.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05336772
Source datasetuspto-grants-1994_08
ORD IDord-d4633577643a4208826e935ea0c9635c
Source noteuspto-grants-1994_08