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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370177Generated: October 30, 2026

Hydrochloric Acid → 1-(Cyclopent-1-en-1-yl)-2,4-difluorobenzene

https://huagongshe.com/reaction/2370177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyclopentanoneHCID 8452—
ReactantHCID 178505836HCID 178505836—
SolventTetrahydrofuranHCID 8028—
Product1-(Cyclopent-1-en-1-yl)-2,4-difluorobenzeneHCID 5807575826.3%

Reaction Steps

To a 0.497M solution of (2,4-difluorophenyl)magnesium bromide (32.4 g, 149 mmol) in THF at 0° C. was carefully added cyclopentanone (13.23 mL, 149 mmol). Upon the end of the addition, the reaction mixture was heated at reflux for 2 h. Ice (10 g) and 6N aqueous hydrochloric acid were added. The reaction mixture was extracted with ether. The combined organic extracts were washed with a saturated aqueous solution of sodium hydrogen sulfite, a saturated aqueous solution of sodium bicarbonate and water. The organic layer was dried over anhydrous magnesium sulfate and filtered. The solvent was removed in vacuum and the residue was purified by column chromatography on silica gel to give 1-cyclopentenyl-2,4-difluorobenzene (7.064 g, 39.2 mmol, 26.3% yield) as colorless oil. LC-MS (M+H)+=181.0. 1H NMR (500 MHz, CDCl3) δ ppm 7.22-7.31 (1H, m), 6.75-6.85 (2H, m), 6.26-6.31 (1H, m), 2.68-2.74 (2H, m), 2.51-2.58 (2H, m), 1.93-2.02 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710061B2
Source datasetuspto-grants-2014_04
ORD IDord-1a9b99c1d1f147dd9e70f34636f4c910
Source noteuspto-grants-2014_04