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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448138Generated: October 27, 2026

1-Bromonaphthalene → 1-Cyclopropylnaphthalene

https://huagongshe.com/reaction/448138

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 numberUS08481581B2
Source datasetuspto-grants-2013_07
ORD IDord-ccdd59be48a541a9a605a6921766dcd4
Source noteuspto-grants-2013_07