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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748559Generated: October 31, 2026

Potassium Carbonate → HCID 86692460, compound

https://huagongshe.com/reaction/1748559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant5-Bromo-2-fluoropyridineHCID 2783168—
Reactant1,4-Dioxaspiro[4.5]decane-8-carbonitrileHCID 11116433—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86692460HCID 8669246064.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 1,4-dioxaspiro[4.5]decane-8-carbonitrile (13.4 g) described in Reference Example 82 (1) was added a 1 M solution of sodium bis(trimethylsilyl)amide in tetrahydrofuran (100 ml), stirred at 0° C., then a solution of 5-bromo-2-fluoropyridine (12.8 g) in tetrahydrofuran (20 ml) was added thereto, and stirred at room temperature for 1 hour. Tetrahydrofuran (20 ml) was added thereto, additionally stirred for 1 hour, then to the reaction solution was added an aqueous solution of potassium carbonate, extracted with ethyl acetate, washed with saturated brine, dried over anhydrous sodium sulfate, and then the solvent was evaporated in vacuo. To the residue were added water (10 ml) and trifluoroacetic acid (50 ml), and stirred at room temperature for 6 hours. The reaction solution was added to an aqueous solution of potassium carbonate, the mixture was extracted with ethyl acetate, the organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified with silica gel column chromatography (n-hexane/ethyl acetate) to give 1-(5-bromopyridin-2-yl)-4-oxocyclohexanecarbonitrile (13.08 g) as a pale yellow solid. MS (ESI) m/z: 279, 281 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-37ba6a365dc7407eb792c3911e8840b3
Source noteuspto-grants-2015_10