HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302095Generated: October 25, 2026
Acetic Acid → 1-Acetyl-3,5-dimethyl Adamantane
https://huagongshe.com/reaction/2302095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Butanedione | HCID 650 | — |
| Reactant | 1,3-Dimethyladamantane | HCID 12800 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Product | 3,5-Dimethyl-1-adamantanol | HCID 265793 | 6% |
| Product | 1-Acetyl-3,5-dimethyl Adamantane | HCID 12113124 | 40% |
| Product | 1,3-Diacetyl-5,7-dimethyladamantane | HCID 12113141 | 15% |
| Product | 1,3-Dimethyl-4-adamantanone | HCID 12644332 | 4% |
Reaction Steps
A mixture of 3 mmol of 1,3-dimethyladamantane, 18 mmol of biacetyl, 0.015 mmol of cobalt (II) acetate, and 3 ml of acetic acid was stirred at 60° C. under an oxygen atmosphere (1 atm) for 4 hours. Gas chromatographic analysis of products in the reaction mixture revealed that 1,3-dimethyladamantane was converted, at a rate of 93%, to 1-acetyl-3,5-dimethyladamantane (yield 40%), 1,3-diacetyl-5,7-dimethyladamantane (yield 15%), 1-acetyl-3,5-d-methyl-7-adamantanol (yield 5%), 1,3-dimethyl-5-adamantanol (yield 6%), and 1,3-dimethyl-4-adamantanone (yield 4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06429314B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-bd1167e0930d4c7e884b10f8d5118839 |
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| Source note | uspto-grants-2002_08 |
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