Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | Idramantone | HCID 64184 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 2843184 | HCID 2843184 | — |
Reaction Steps
A solution of 5-hydroxy-2-adamantanone (2.6 g, 15.66 mmoles) in dichloromethane (DCM)(50 mL) was treated with dimethylaminopyridine (DMAP)(2.1 g, 17 mmoles) and acetic anhydride (2.3 mL, 23 mmoles) and stirred overnight at 50° C. The solvent was removed under reduced pressure and the residue was partitioned between water and ethyl acetate. The aqueous layer was extracted twice with ethyl acetate. Combined organic extracts were washed with water, dried (MgSO4) and filtered. The filtrate was concentrated under reduced pressure to provide the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880001B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-1704e4f554be426d8133a5cf9420375d |
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| Source note | uspto-grants-2011_02 |
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