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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805741Generated: November 1, 2026

1-Iodonaphthalene → HCID 67381530, compound

https://huagongshe.com/reaction/1805741

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodonaphthaleneHCID 7004—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 44204091HCID 44204091—
CatalystPalladium ChlorideHCID 24290—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 67381530HCID 67381530137.5%

Reaction Steps

12 ml of THF/H2O was added to 0.6199 g (2.44 mmol) of iodonaphthalene, and 0.122 g (5 mol %) of PdCl2 (dppf) was added in a darkroom. 1 g (2.44 mmol) of 3,5-bis-tert-butyldimethylsilyloxymethyl Phenylboronic acid dissolved in 12 ml of THF/H2O was added, 3.66 ml (3 eq) of 2N NaOH aq was injected, the reaction was initiated in a 65° C. oil bath with light shielding, and the mixture was agitated for 24 hours. Completion of the reaction could not be confirmed because the raw material iodonaphthalene overlaps the target product in TLC (Hex only). Fluorescence was confirmed with the naked eye. This was extracted with EtOAc, and the organic layer was washed with H2O, sat. NaHCO3 aq and sat. NaCl aq, and dried by addition of anhydrous NaSO4. The solvent was distilled off under reduced pressure to obtain 1.6530 g of a mixture of the target product and iodonaphthalene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354515B2
Source datasetuspto-grants-2013_01
ORD IDord-9973e381cfcf4404a8d14b12c9479a13
Source noteuspto-grants-2013_01