HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381777Generated: October 27, 2026
(Anthracen-1-yl)methanol → Anthracenecarboxaldehyde
https://huagongshe.com/reaction/1381777
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Anthracen-1-yl)methanol | HCID 12695455 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Anthracenecarboxaldehyde | HCID 35864 | 67.9% |
Reaction Steps
To a 2 L round bottom flask equipped with condenser and magentic stirring bar was added (1-anthracenyl)methanol (15C, 21.0 g, 0.10 mol), CH2Cl2 (1200 mL) and pyridinium chlorochromate (PCC) (Aldrich, 32.33 g, 0.15 mol). The mixture was then refluxed for 5 h. The reaction was cooled and then filtered through a plug of silica gel (400 g) using PhCH3 as eluting solvent. The first 1 L of solution was collected and concentrated to give 16 g of crude product. This material was further purified by preparative HPLC using PhCH3 as eluting solvent. The solvent was removed and the resulting solid recrystallized (PhCH3 /hexane) to give 14.0 g (67%) of 1-anthracenecarbaldehyde mp 130°-131.5°, (C, H), (lit. mp 126.5°-127.5°, P. H. Gore J. Chem. Soc. 1616 (1959)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04803221 |
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| Source dataset | uspto-grants-1989_02 |
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| ORD ID | ord-102135cd8b234d1691ab6a98fb2e4b97 |
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| Source note | uspto-grants-1989_02 |
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