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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844257Generated: November 1, 2026

1-Bromonaphthalene → 1-Cyclopropylnaphthalene

https://huagongshe.com/reaction/1844257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromonaphthaleneHCID 7001—
ReactantHCID 178418630HCID 178418630—
CatalystHCID 178418745HCID 178418745—
SolventTetrahydrofuranHCID 8028—
Product1-CyclopropylnaphthaleneHCID 1466869376%

Reaction Conditions

Temperature0 °C

Reaction Steps

Cyclopropylmagnesium bromide (150 mL, 0.5 M in tetrahydrofuran) was slowly added to a solution of 1-bromo-naphthalene (10 g, 50 mmol) and [1,3-bis(diphenylphosphino)propane]dichloronickel(II) in tetrahydrofuran (10 mL) stirred at 0° C. The reaction mixture was stirred at room temperature for 16 hours and the solvent was evaporated under reduced pressure. EtOAc and ammonium chloride in water were added. After extraction, the organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography to yield 1-cyclopropyl-naphthalene (6.4 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946273B2
Source datasetuspto-grants-2015_02
ORD IDord-f37b11f4a9464732b8b8b3686e0eed08
Source noteuspto-grants-2015_02