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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474267Generated: October 25, 2026

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

https://huagongshe.com/reaction/474267

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 0.497 M 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 6 N 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 vacuo 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 a 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 numberUS08637523B2
Source datasetuspto-grants-2014_01
ORD IDord-57c39693741a4d50b36f0e9415477f39
Source noteuspto-grants-2014_01