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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853127Generated: November 2, 2026

Water → 1-(3-Fluoropyridin-2-yl)-3-oxocyclobutane-1-carbonitrile

https://huagongshe.com/reaction/1853127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-(3-Fluoropyridin-2-yl)-3-methylenecyclobutane-1-carbonitrileHCID 67451030—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product1-(3-Fluoropyridin-2-yl)-3-oxocyclobutane-1-carbonitrileHCID 6745314186.3%

Reaction Conditions

Temperature15 °C

Reaction Steps

To a mixture of 1-(3-fluoropyridin-2-yl)-3-methylenecyclobutanecarbonitrile (272 g, 1.45 mol) and RuCl3.H2O (9.0 g, 0.044 mol) in DCM (1 L), acetonitrile (1 L), and water (1.5 L) mixture was added solid NaIO4 (1235 g, 5.8 mol) portionwise at 10-30° C. Upon the completion of addition, the reaction was stirred 1 h at 15° C. and overnight at rt. The solid precipitate was filtered off and washed with DCM (2×1000 mL). The organic layer was washed with water (2×500 mL) and brine (500 mL), dried over Na2SO4, and concentrated to provide a crude title compound as a dark solid (238 g, 86.3%). LRMS (M+H+) m/z 191.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962632B2
Source datasetuspto-grants-2015_02
ORD IDord-2d0b45f360f54245ab6c9d7323dc7e37
Source noteuspto-grants-2015_02