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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381777Generated: October 27, 2026

(Anthracen-1-yl)methanol → Anthracenecarboxaldehyde

https://huagongshe.com/reaction/1381777

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Anthracen-1-yl)methanolHCID 12695455—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductAnthracenecarboxaldehydeHCID 3586467.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803221
Source datasetuspto-grants-1989_02
ORD IDord-102135cd8b234d1691ab6a98fb2e4b97
Source noteuspto-grants-1989_02