HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3aR,4R,5R,6aS)-4-formyl-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl benzoate → (1S,5R,6R,7R)-7-benzoyloxy-6-[(1E)-3-oxo-1-octen-5-ynyl]-2-oxabicyclo[3.3.0]octan-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3aR,4R,5R,6aS)-4-formyl-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl benzoate | HCID 11000244 | — |
| Reactant | HCID 20448678 | HCID 20448678 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (1S,5R,6R,7R)-7-benzoyloxy-6-[(1E)-3-oxo-1-octen-5-ynyl]-2-oxabicyclo[3.3.0]octan-3-one | HCID 70481263 | 98.1% |
Reaction Steps
A solution of 7.4 g of (1S,5R,6R,7R)-6-formyl-7-benzoyloxy-2-oxabicyclo[3.3.0]octan-3-one (E. J. Corey et al., J. Chem. Soc., 91, 5675 (1969)) and 10.3 g of the phosphorane prepared in Example (23b) in 200 ml of absolute toluene is stirred at room temperature for 5.5 hours. The reaction solution is concentrated in vacuo and the residue is chromatographed over silica gel by gradient elution in hexane/40% ethyl acetate. 9.7 g of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04466969 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-a9a2d6feca93422588ebb0a6f20cc127 |
| Source note | uspto-grants-1984_08 |