HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270736Generated: October 25, 2026
Potassium Carbonate → 9-(2-Naphthyl)-10-triphenysilyl anthracene
https://huagongshe.com/reaction/270736
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (Naphthalen-2-yl)boronic acid | HCID 2734375 | — |
| Reactant | 9-Bromo-l0-triphenysilyl anthracene | HCID 59833959 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 9-(2-Naphthyl)-10-triphenysilyl anthracene | HCID 59833958 | — |
Reaction Steps
9-bromo-10-triphenysilyl anthracene (4 g, 7.8 mmol), 2-naphthylboronic acid (1.6 g, 9.4 mmol) and K2CO3 (1.5 g,15.6 mmol) were dissolved in the solvent mixture of 50 mL ethylene glycol dimethyl ether and 75 mL water. The stirred solution was added tetrakis (triphenylphosphine) palladium (0) and the mixture refluxed under N2 for 16 hours. The reaction mixture was cooled and the water extracted with acetyl acetate three times. The combined organic phase was washed with portions of brine. The organic layer was then dried with MgSO4, filtered, and evaporated of solvent. The crude material was purified by column chromatography (n-hexane/acetyl acetate=10/1) to give 9-(2-naphthyl)-10-triphenysilyl anthracene (Compound 2), the reaction was following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449593B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-593ab732c5ec421ba75b5e0d6f386ad3 |
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| Source note | uspto-grants-2008_11 |
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