HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770180Generated: October 31, 2026
Trifluoromethanesulfonic acid → 2-Fluoro-4-(5-decylpyrimidine-2-yl)phenyl triflate
https://huagongshe.com/reaction/1770180
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | 2-Fluoro-4-(5-decylpyrimidine-2-yl)phenol | HCID 135811206 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Fluoro-4-(5-decylpyrimidine-2-yl)phenyl triflate | HCID 20095052 | 94.3% |
Reaction Steps
1.00 g (3.03 mM) of 2-fluoro-4-(5-decylpyrimidine-2-yl)phenol, 3 ml of pyridine were mixed and stirred on a common salt-ice bath. To the mixture, 1.00 ml (5.94 mM) of anhydrous trifluoromethanesulfonic acid was added dropwise and stirred for 20 minutes, followed by further stirring for 70 minutes at room temperature. After the reaction, the reaction mixture was left standing overnight and then 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 1.32 g of 2-fluoro-4-(5-decylpyrimidine-2-yl)phenyl triflate (Yield: 94.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05385692 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-58534bdebaaa4e00922f2321a39dc071 |
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| Source note | uspto-grants-1995_01 |
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