HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 9-(Ethoxymethyl)anthracene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 9-(Chloromethyl)anthracene | HCID 32385 | — |
| Product | 9-(Ethoxymethyl)anthracene | HCID 12843200 | — |
Reaction Steps
A solution of 9-chloromethylanthracene (5.2 g, 23 mmole) obtained in Synthesis Example 2-(1) in ethanol (700 ml) was reacted with stirring for 10 hours at room temperature, poured into H2O (700 ml), and extracted with methylene chloride (500 ml×1). The resulting organic layer was dried over anhydrous MgSO4 and evaporated. The residual crude solid (4.25 g) was recrystallized from 50% THF/H2O to give 4.02 g of 9-ethoxymethylanthracene as orange yellow crystals, mp. 74°-75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05695910 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-8576b3b4f74646bcbbda171e97be9fcf |
| Source note | uspto-grants-1997_12 |