HuagongsheHuagongshe Chemistry Print Report · For research reference only
Idramantone → HCID 57429709, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Idramantone | HCID 64184 | — |
| Reactant | 3,3-Dimethylbutanoyl chloride | HCID 81514 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57429709 | HCID 57429709 | — |
Reaction Steps
A solution of 1.03 g of 5-hydroxy-2-adamantanone, 1.83 g of DMAP and 1.9 ml of 3,3-dimethylbutanoyl chloride in 10 ml of CH2Cl2 is stirred at 40° C. for 48 hours, 6 ml of aqueous 1M KH2PO4 solution are added and the mixture obtained is stirred. The layers obtained are separated, from the organic layer obtained solvent is evaporated and the evaporation residue obtained is subjected to chromatography. 3,3-Dimethyl-butyric acid 4-oxo-adamantan-1-yl ester in the form of an oil is obtained. 13C-NMR: 215.61, 171.52, 49.10, 47.02, 41.38, 39.93, 38.17, 30.74, 29.79, 29.62.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07482462B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-6753a510a768447bb2a699a93d124526 |
| Source note | uspto-grants-2009_01 |