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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403306Generated: October 28, 2026

Pyridine, hydrofluoride (1:1) → HCID 59625893, compound

https://huagongshe.com/reaction/403306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine, hydrofluoride (1:1)HCID 64774—
ReactantSelectfluorHCID 2724933—
ReactantHCID 59625898HCID 59625898—
SolventDichloromethaneHCID 6344—
SolventHCID 178435160HCID 178435160—
ProductHCID 59625893HCID 59625893—

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor) (381 mg, 1.07 mmol) and HF-pyridine reagent (1.5 mL, HF:Pyridine=70:30 wt %) were dissolved in CH2Cl2 (4 mL) in a polyethylene bottle and cooled to 0° C. A solution of compound 18b (162 mg, 0.512 mmol) in CH2Cl2 (2 mL) was slowly added and the mixture was stirred for 45 min at room temperature. The solution was extracted with CH2Cl2, and the combined organics were dried over anhydrous Na2SO4 and concentrated. A crude product was purified by flash column chromatography (silica gel, 5% EtOAc/hexanes) to afford compound 18c as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748417B2
Source datasetuspto-grants-2014_06
ORD IDord-2fcad731f42c4bcc820b327965c9d861
Source noteuspto-grants-2014_06