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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474102Generated: November 1, 2026

3-Methylenecyclobutanecarbonitrile → 1-(3-Fluoropyridin-2-yl)-3-methylenecyclobutane-1-carbonitrile

https://huagongshe.com/reaction/1474102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylenecyclobutanecarbonitrileHCID 27474—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant2-Chloro-3-fluoropyridineHCID 2782791—
SolventTolueneHCID 1140—
Product1-(3-Fluoropyridin-2-yl)-3-methylenecyclobutane-1-carbonitrileHCID 6745103089,767.898%

Reaction Steps

To a solution of 3-methylenecyclobutanecarbonitrile (150 g, 1.61 mol, 1 equiv) and 2-chloro-3-fluoropyridine (212 g, 1.61 mmol, 1 equiv) in toluene (1 L) was added NaHMDS (2 M in THF, 885 mL, 1.1 equiv) dropwise at 0-10° C. Upon completion of addition, the reaction mixture was warmed to rt, stirred overnight, and quenched with NH4Cl(sat.) solution. The organic layer was washed with water (2×500 mL) and brine (500 mL), dried over Na2SO4, filtered, and concentrated to give the crude title compound (272 g, 90%) which was used in next step without further purification. LRMS (M+H+) m/z 189.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018223B2
Source datasetuspto-grants-2015_04
ORD IDord-033270ef1de547d0b3b8f8979ff746b0
Source noteuspto-grants-2015_04