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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369183Generated: October 31, 2026

Anthracene → CID 10867395

https://huagongshe.com/reaction/1369183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthraceneHCID 8418—
ReactantMagnesiumHCID 5462224—
Catalyst1,2-DibromoethaneHCID 7839—
SolventTetrahydrofuranHCID 8028—
ProductCID 10867395HCID 10867395—

Reaction Steps

2.7 g (110 mmol) of magnesium turnings were added to a solution of 2 g (11 mmol) of anthracene in 100 ml of THF, and a few drops of 1,2-dibromoethane were added. After the mixture had been stirred at room temperature for about 2 hours, the bright orange precipitate of magnesium anthracene had formed. A solution of 19 g (100 mmol) of 4-chlorobenzaldehyde dimethyl acetal in 100 ml of THF was added to the refluxing suspension over the course of 1 hour. After the mixture had refluxed for 4 hours, the yield of Mg 4-chlorobenzaldehyde dimethyl acetal according to GC analysis (determined as benzaldehyde after hydrolysis using dilute HCl) was 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576789B1
Source datasetuspto-grants-2003_06
ORD IDord-693242eb204c4b3e9f5f35d08ace2259
Source noteuspto-grants-2003_06