HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 3-(1-Adamantyl)-4-methoxybenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Methoxybenzoic Acid | HCID 7478 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 1-Adamantyl acetate | HCID 519973 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(1-Adamantyl)-4-methoxybenzoic acid | HCID 5296503 | — |
Reaction Steps
In a 100 ml three-necked flask, and under a nitrogen environment, are placed 1 g of 1-acetoxyadamantane and 50 ml of n-heptane. After dissolution, 0.25 g of concentrated sulfuric acid is added drop by drop at a temperature of approximately 22° C. and 0.783 g of 4-methoxybenzoic acid is poured in slowly. After leaving the mixture well agitated for 48 hours, 50 ml of denatured ethanol are added and the insoluble material is filtered Concentration of the filtrate volume to three quarters yields a solid white precipitate which is filtered with sintered glass. It is dried in a vacuum oven for 24 hours at 30° C. and 0.680 g of expected raw product was collected (Melting point: 245°-246° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05015758 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-b57f06557a5d4955b526d18a5473bbc9 |
| Source note | uspto-grants-1991_05 |