HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051081Generated: October 31, 2026
Sulfuric Acid → 2-(1-Adamantyl)-4-bromophenol
https://huagongshe.com/reaction/2051081
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 1-Adamantyl acetate | HCID 519973 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(1-Adamantyl)-4-bromophenol | HCID 4670494 | — |
Reaction Steps
In a 100 ml three-necked flask, and under a nitrogen environment, is placed 1 g of 1-acetoxyadamantane and 10 ml of n-heptane. After total dissolution, 0.25 g of concentrated sulfuric acid is added drop by drop while keeping the temperature at 20° C., then 0.886 g of 4bromophenol is poured in slowly. After leaving 24 hours in vigorous agitation, 20 ml of denatured ethanol are added while maintaining the temperature at 20° C. Next, the solvent is evaporated to dryness under reduced pressure and a whitish raw product is obtained. The product is redissolved in water at approximately 60° C., it is washed to pH 6 and dried in a vacuum oven for 24 hours at 25° C. One collected 1.24 g of expected raw product (Melting point: 140°-141° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05015758 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-8e8b0194384242f78c15282a4df3a6d0 |
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| Source note | uspto-grants-1991_05 |
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