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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181921Generated: October 31, 2026

Pyridine → 4-tert-Butyl-2-nitrophenyl trifluoromethanesulfonate

https://huagongshe.com/reaction/1181921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenol, 4-(1,1-dimethylethyl)-2-nitro-HCID 18661—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product4-tert-Butyl-2-nitrophenyl trifluoromethanesulfonateHCID 2310901587%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triflic anhydride (4.14 mL, 24.6 mmol) was added dropwise to a solution of 4-tert-butyl-2-nitrophenol (4.00 g, 20.5 mmol) and pyridine (2.16 mL, 26.7 mmol) in methylene chloride (50 mL) at 0° C. The yellow solution was stirred 0.25 h at 0° C., poured onto saturated aqueous NaHCO3 and extracted with methylene chloride. The combined extracts were washed with saturated aqueous NaHCO3, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by filtration through a plug of silica-gel (methylene chloride) to provide trifluoro-methanesulfonic acid 4-tert-butyl-2-nitro-phenyl ester (5.82 g, 87%) as a pale yellow oil which was utilized without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285545B2
Source datasetuspto-grants-2007_10
ORD IDord-d9804a7043f54951a63815cb7e49e5ae
Source noteuspto-grants-2007_10