HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → HCID 14549073, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 2-Bromo-6-methoxynaphthalene | HCID 78786 | — |
| Reactant | 1-Adamantyl acetate | HCID 519973 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14549073 | HCID 14549073 | 20.9% |
Reaction Steps
In a 100 ml flask, under a nitrogen atmosphere, are placed 1 g of 1-acetoxyadamantane and 30 ml of n-heptane, and 0.25 g of concentrated sulfuric acid is introduced. At a temperature of about 20° C., 1.22 g of 2-bromo-6-methoxynaphthalene are poured in slowly and the mixture is left in vigorous agitation for 48 hours. Next, 20 ml of denatured ethanol are introduced and the mixture is evaporated to dryness under reduced pressure. The product is taken up in denatured ethanol and the precipitate is filtered with sintered glass. After drying of the raw product in a vacuum oven for 24 hours at 30° C., one purifies using silica column chromatography. There were obtained 0.4 g of the desired raw product (Melting point: 164°-168° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05015758 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-c95db27efb8940b093a879dbaa879e0d |
| Source note | uspto-grants-1991_05 |