HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916909Generated: October 30, 2026
Vinyl Acetate → 5-(Ethenyloxy)tricyclo[3.3.1.1~3,7~]decane-1,3-diol
https://huagongshe.com/reaction/916909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vinyl Acetate | HCID 7904 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,3,5-Adamantanetriol | HCID 9899022 | — |
| Reactant | HCID 22034515 | HCID 22034515 | — |
| Reactant | HCID 22034538 | HCID 22034538 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(Ethenyloxy)tricyclo[3.3.1.1~3,7~]decane-1,3-diol | HCID 22034574 | — |
Reaction Steps
To a mixture of di-μ-chlorobis(1,5-cyclooctadiene)diiridium(I) [Ir(cod)Cl]2 (6.7 mg, 0.01 mmol) and sodium carbonate (64 mg, 0.6 mmol) in toluene (1.0 ml), 1,3,5-adamantanetriol (1 mmol) and vinyl acetate (9 mmol) were added, followed by stirring at 100° C. in an atmosphere of argon gas for 5 hours. The reaction mixture was analyzed by gas chromatography to find that 1,3,5-tris(vinyloxy)adamantane, 3,5-bis(vinyloxy)-1-adamantanol, and 5-vinyloxy-1,3-adamantanediol were produced in yields of 52%, 18%, and 8%, respectively, with a conversion from 1,3,5-adamantanetriol of 97%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07271297B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-a8aefcb8ba3842608d8c6ec5126b1ed9 |
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| Source note | uspto-grants-2007_09 |
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