HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179867Generated: October 31, 2026
Pyridinium chloride → HCID 86701364, compound
https://huagongshe.com/reaction/2179867
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | HCID 86701362 | HCID 86701362 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 86701364 | HCID 86701364 | 99.5% |
Reaction Steps
Under the nitrogen atmosphere, 9-(7-methoxynaphthalen-2-yl)-10-(4-phenylnaphthalen-1-yl)anthracene (16.0 g) as the twentieth intermediate compound, pyridine hydrochloride (17.3 g) and N-methylpyrrolidone (30 ml) were added to a flask and stirred for 8 hours at 200° C. Once the heating is completed, the mixture was cooled to 100° C. or lower. Liquid separation was performed by adding water and toluene. The solvent was distilled off under reduced pressure and the resulting solid was purified by silica gel column chromatography (solvent: toluene) to give 7-(10-(4-phenylnaphthalen-1-yl)anthracen-9-yl)naphthalen-2-ol (15.5 g) as a twenty-first intermediate compound. The scheme is shown in the following “Reaction 33”.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09070885B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-e96d3a8eb50d4555928d49a536b5dc0e |
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| Source note | uspto-grants-2015_06 |
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