HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 54475024, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 1,8-Dihydroxybicyclo[7.3.1]trideca-4,9-diene-2,6-diyn-13-one | HCID 54127051 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 54475024 | HCID 54475024 | 85% |
Reaction Steps
To a solution of 1,8-dihydroxy-bicyclo[7.3.1]trideca-4,9-diene-2,6-diyn-13-one (product of Example 4, 32 mg, 0.149 mmol) in 1 ml of pyridine Was added dimethylaminopyridine and 1 eq of acetic anhydride (14 ul, 0.149 mmol). The reaction mixture was stirred at ambient temperature for 30 minutes and then pyridine was stripped off on rotovap and on high vacuum. This residue was purified on a silica gel column using 10% and 20% ethyl acetate/hexane mixture as the solvent system. The title compound was obtained as light yellow foam in 85% yield (32.4 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05198560 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-4a17fb3540534e01a8ae4a4fd8dc44b2 |
| Source note | uspto-grants-1993_03 |