HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 22463561, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 1,3-Adamantanediol | HCID 573829 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22463561 | HCID 22463561 | 90% |
Reaction Steps
In an atmosphere of nitrogen, 10 mmole of 1,3-adamantanediol and 24 mmole of pyridine were dissolved in 10 mL of DMF. To the mixture, 22 mmole of methoxycarbonyl chloride was added dropwise with stirring at room temperature. 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-adamantanediol was 99% and 1,3-bis (methoxycarbonyloxy)adamantane (yield 90%) was formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06392104B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-1bb26664d2ba41b0907e20ccf76ad2c7 |
| Source note | uspto-grants-2002_05 |