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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770182Generated: October 31, 2026

Trifluoromethanesulfonic acid → 3-Fluoro-4-(5-decylpyrimidine-2-yl)phenyl triflate

https://huagongshe.com/reaction/1770182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
Reactant3-Fluoro-4-(5-decylpyrimidine-2-yl)phenolHCID 135757337—
SolventPyridineHCID 1049—
Product3-Fluoro-4-(5-decylpyrimidine-2-yl)phenyl triflateHCID 2009501099.1%

Reaction Steps

1.80 g (2.42 mM) of 3-fluoro-4-(5-decylpyrimidine-2-yl)phenol, 2.42 ml of pyridine were mixed and stirred on a common salt-ice bath. To the mixture, 0.80 ml (4.76 mM) of anhydrous trifluoromethanesulfonic acid was added dropwise and stirred for 20 minutes, followed by further stirring for 140 minutes at room temperature. After the reaction, the reaction mixture was poured into ice water, followed by extraction with isopropyl ether. The isopropyl ether layer was successively washed with a common salt aqueous solution, 12%-HCl and a common salt aqueous solution, followed by drying with anhydrous sodium sulfate. The sodium sulfate was removed by filtration and the filtrate was concentrated into a solid product, whereby 1.11 g of 3-fluoro-4-(5-decylpyrimidine-2-yl)phenyl triflate (Yield: 99.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05385692
Source datasetuspto-grants-1995_01
ORD IDord-c9ead2229a3847699ffdc4a725b71ab4
Source noteuspto-grants-1995_01