HuagongsheHuagongshe Chemistry Print Report · For research reference only
Anthracene → CID 10867395
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Anthracene | HCID 8418 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | 1,2-Dibromoethane | HCID 7839 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | CID 10867395 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06576789B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-693242eb204c4b3e9f5f35d08ace2259 |
| Source note | uspto-grants-2003_06 |