HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 9-(Chloromethyl)anthracene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 9-Anthracenemethanol | HCID 73848 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 9-(Chloromethyl)anthracene | HCID 32385 | 94.1% |
Reaction Steps
To a suspension of 9-anthracenemethanol (50 g, 0.24 mole) in methylene chloride (50 ml), a solution of thionyl chloride (32.3 g, 0.27 mole) in benzene (300 ml) was added, and reacted with stirring for 10 hours under reflux. The reaction mixture was poured into ice-water (500 ml). An organic layer separated was washed with H2O (100 ml×3), dried over anhydrous MgSO4 and evaporated to give 51.2 g of 9-chloromethylanthracene as residual crude orange yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05695910 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-3d9d14dae93b40d8aaf71a520382401e |
| Source note | uspto-grants-1997_12 |