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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518596Generated: October 31, 2026

Acetonitrile → HCID 583430, compound

https://huagongshe.com/reaction/1518596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2-Bromo-5-methylpyridineHCID 564216—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 583430HCID 583430234.3%

Reaction Conditions

Temperature78 °C

Reaction Steps

To a solution of anhydrous acetonitrile (10.1 mL, 191.83 mmol, 3.3 equiv.) in dry THF (500 mL) was added dropwise n-butyl lithium (2.5 M in hexane, 69.8 mL, 174.39 mmol, 3 equiv.) at minus 78° C. under a nitrogen atmosphere. The resulting white suspension was stirred at minus 78° C. for 1 hour, and then a solution of 2-bromo-5-methylpyridine (10.0 g, 58.13 mmol, 1 equiv.) in dry THF (30 mL) was added. The reaction mixture was kept at minus 78° C. for 1 hour and then warmed up slowly to room temperature and stirred for another hour. Ice/water was added and the layer was separated. The organic layer was washed with water and brine, dried over MgSO4, filtered, and evaporated to give 18 g of crude product, which was used for next step reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09072313B2
Source datasetuspto-grants-2015_07
ORD IDord-6f390e37b14a4008b2a673f8b0fed084
Source noteuspto-grants-2015_07