HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Tricyclo(3.3.1.13,7)dec-1-yl-1-naphthalenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | 1-Adamantyl acetate | HCID 519973 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | 2-Tricyclo(3.3.1.13,7)dec-1-yl-1-naphthalenol | HCID 19834508 | 20.7% |
Reaction Steps
A three-necked 100 ml flask is charged with 2.7 g of 1-acetoxyadamantane and 5 ml of cyclohexane in a nitrogen atmosphere. After complete dissolution, there are introduced 1.4 g of concentrated sulfuric acid. In a single portion there is added a suspension of 2 g of 1-naphthol in 15 ml of cyclohexane and one agitates for 45 minutes. 20 ml of ethanol are added and the mixture is filtered. One washes the residue with ethanol and with water and dries on the filter. After recrystallization with cyclohexane, one obtained 0.8 g of the desired product melting at 209.2°-209.6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05015758 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-62f4e1c95f6c48939dd75d78f8726d6f |
| Source note | uspto-grants-1991_05 |