Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,3,5-Adamantanetriol | HCID 9899022 | — |
| Product | HCID 22463562 | HCID 22463562 | 95% |
Reaction Steps
In an atmosphere of nitrogen, 10 mmole of 1,3,5-adamantanetriol obtained by the method of Example 32 and one drop of pyridine were dissolved in 10 mL of DMF. To the mixture, 30 mmole of methylisocyanato was added dropwise with stirring. Cooling of the resultant mixture with ice was started at about the time exothermic reaction began. When the exothermic reaction is completed, the mixture was heated to 60° C. and then stirred for one hour. As a result, the conversion of 1,3,5-adamantanetriol was 99% and 1,3,5-tris(methylcarbamoyloxy)adamantane (yield 95%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE039744E1 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-afe5608e102f414788e9028dfad6a3e7 |
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| Source note | uspto-grants-2007_07 |
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