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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897572Generated: October 30, 2026

Pyridine → 6-Bromonaphthalene-2-carbonitrile

https://huagongshe.com/reaction/1897572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant6-Bromo-2-naphthamideHCID 57428037—
Solvent1,4-DioxaneHCID 31275—
Product6-Bromonaphthalene-2-carbonitrileHCID 1466211570.3%

Reaction Steps

To 6-bromo-2-naphthamide (1 g, 4.00 mmol) in 1,4-dioxane (8.00 ml) at 0° C. was added pyridine (0.647 ml, 8.00 mmol) and then trifluoroacetic anhydride (0.621 ml, 4.40 mmol) dropwise. The reaction was stirred at room temperature for 3 h. The mixture was quenched with H2O and extracted with EtOAc two times, dried over magnesium sulfate, filtered, concentrated. The title compound 2b (653 mg, 70%) was isolated as beige solid, and used as is for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519134B2
Source datasetuspto-grants-2013_08
ORD IDord-a1d4e32b48004eb18d0f93ce01f6e90a
Source noteuspto-grants-2013_08