HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 76381099, compound → HCID 13914416, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 76381099 | HCID 76381099 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 13914416 | HCID 13914416 | 94% |
Reaction Steps
To 1.1 g of platinium in 50 ml of ethyl acetate was added a solution of 11 g (0.028 mol) of [3aR-[3a alpha,4alpha(1E,3R*,4S*),5beta,6a alpha]]-5-(benzoyloxy)-4-(4-fluoro-3-hydroxy-1-octenyl)hexahydro-2H-cyclopenta[b]furan-2-one in 110 ml of ethyl acetate. The mixture was then hydrogenated until the theoretical uptake of hydrogen was complete and then filtered through a bed of Celite. The solvent was then removed under reduced pressure and the residue chromatographed over 250 g of silica gel (toluene --α 30% by volume ethyl acetate/70% by volume toluene) to afford 10.7 g of [3aR-[3a alpha,4alpha(3R*,4S*),5beta,6a alpha)]-5-(benzoyloxy)-4-(4-fluoro-3-hydroxyoctyl)hexahydro-2H-cyclopenta[b]furan-2-one (94% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04634782 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-eca0971ae6d64d469051a34919fc2d2a |
| Source note | uspto-grants-1987_01 |