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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555834Generated: October 27, 2026

Water → 3-(3-Fluoropyrazin-2-yl)cyclohex-2-enone

https://huagongshe.com/reaction/555834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2-Fluoro-3-iodopyrazineHCID 15369693—
Reactant3-(Tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-2-en-1-oneHCID 57496422—
CatalystHCID 178418903HCID 178418903—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-(3-Fluoropyrazin-2-yl)cyclohex-2-enoneHCID 59351405—

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Fluoro-3-iodopyrazine (2.5 g, 11.16 mmol), 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-2-enone (3.10 g, 13.95 mmol), and sodium carbonate (3.55 g, 33.5 mmol) were suspended in DME (20 ml) and distilled water (5 ml). Argon was bubbled through the resulting mixture for 3 minutes, and dichlorobis(triphenylphosphino)palladium (ii) (0.431 g, 0.614 mmol) was added. The resulting mixture was stirred at 80° C. for 16 hours, the reaction was cooled to RT, and water (200 ml) was added. The resulting mixture was concentrated under reduced pressure and was extracted with EtOAc (3×200 ml). The combined organic layers were washed with brine and dried over sodium sulfate. Filtration and concentration under reduced pressure, followed by flash chromatography on silica gel (0% to 20% EtOAc in hexanes) afforded 3-(3-fluoropyrazin-2-yl)cyclohex-2-enone as a light yellow solid. MS (ESI, pos. ion) m/z: 193.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053438B2
Source datasetuspto-grants-2011_11
ORD IDord-8172ce7bca3c4e21aba86980dc61dd7b
Source noteuspto-grants-2011_11