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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077043Generated: November 1, 2026

Pyridine → HCID 59312242, compound

https://huagongshe.com/reaction/2077043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 135741926HCID 135741926—
SolventDichloromethaneHCID 6344—
ProductHCID 59312242HCID 5931224297.5%

Reaction Steps

Triflic anhydride (516 mg, 0.30 mL, 1.83 mmol) was added dropwise to a solution of the product of Step A (500 mg, 1.41 mmol) and pyridine (167 mg, 0.17 mL, 2.11 mmol) in CH2Cl2 (5.0 mL) at 0° C. The resulting solution was allowed to warm to room temperature and stirred for 1 h. The reaction mixture was quenched by addition of water then partitioned between 5% citric acid and ethyl acetate. The organic layer was washed with sodium bicarbonate (sat.), dried over magnesium sulfate and concentrated under vacuum to yield the crude product as a yellow gum (670 mg). This material was taken on without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928099B2
Source datasetuspto-grants-2011_04
ORD IDord-7adfcc3bbf8f49a89618c162c5779c8e
Source noteuspto-grants-2011_04