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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614730Generated: October 30, 2026

Acetic Anhydride → HCID 54475024, compound

https://huagongshe.com/reaction/1614730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant1,8-Dihydroxybicyclo[7.3.1]trideca-4,9-diene-2,6-diyn-13-oneHCID 54127051—
SolventPyridineHCID 1049—
ProductHCID 54475024HCID 5447502485%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198560
Source datasetuspto-grants-1993_03
ORD IDord-4a17fb3540534e01a8ae4a4fd8dc44b2
Source noteuspto-grants-1993_03