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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051956Generated: November 3, 2026

Norbornadiene → HCID 90303209, compound

https://huagongshe.com/reaction/1051956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNorbornadieneHCID 8473—
Reactant2-Cyclopenten-1-oneHCID 13588—
ReactantN-bromobutanimideHCID 67184—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantGadolinium triflateHCID 11114694—
CatalystBis(1,5-cyclooctadiene)nickelHCID 6433264—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90303209HCID 90303209—

Reaction Steps

Bicyclo[2.2.1]hepta-2,5-diene (0.84 g, 9.14 mmol), followed by Gd(OTf)3 (1.84 g, 3.05 mmol), 2-cyclopenten-1-one (5.00 g, 60.9 mmol) and TMS-CN (9.25 g, 91.4 mmol) were added to a degassed solution of Ni(cod)2 (0.84 g, 3.04 mmol) in THF (160 mL) and the mixture was stirred at RT for 4 h. Subsequently, the mixture was quenched with solid NaHCO3 and aq. sat. NaHCO3 and extracted with EtOAc. The comb. org. layers were washed with brine, dried over MgSO4 and conc. in vacuo. The residue, a yellow oil, was dissolved in THF/H2O (450 mL, 9:1). At 0° C., NBS (11.98 g, 67.3 mmol) was added and the mixture was stirred at 0° C. for 30 min. Subsequently, the mixture was quenched with aq. sat. Na2SO3 and extracted with EtOAc. The comb. org. layers were washed with aq. 5% NaHCO3 and brine, dried over Na2SO4, and conc. in vacuo. The residue was re-dissolved in EtOAc, washed multiple times with aq. 5% NaHCO3 and brine, the combined org. layer were dried over Na2SO4, and conc. in vacuo to provide a brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388198B2
Source datasetuspto-grants-2016_07
ORD IDord-f02655b8c2eb47fc8ceb61cba0ae9374
Source noteuspto-grants-2016_07