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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209094Generated: November 4, 2026

Trifluoromethanesulfonic anhydride → Pyridin-4-yl trifluoromethanesulfonate

https://huagongshe.com/reaction/2209094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 178504229HCID 178504229—
SolventDichloromethaneHCID 6344—
ProductPyridin-4-yl trifluoromethanesulfonateHCID 18424478123.3%

Reaction Steps

To solution of 2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-4-yl)pyridin-4-ol (0.67 g, 2 mmol) in DCM was added TEA (0.69 g, 7 mmol) and the mixture was stirred at OC, (Tf)2O (0.843 g, 3 mmol) was added slowly. The resulting reaction mixture was steered at r.t. for one hour. Solvent was removed under vacuo. And the residue was purified by silicone gel column to afford 2414(2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-4-yl)pyridin-4-yl trifluoromethanesulfonate (0.56 g, 58%) LCMS-ESI+ (m/z): [M+H]+ calcd. for C26H30N5O3: 424.48; found: 424.05.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376441B2
Source datasetuspto-grants-2016_06
ORD IDord-f56aa9bd71e64ea78772f7fc41e78be0
Source noteuspto-grants-2016_06