HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049954Generated: October 26, 2026
Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate → (3aR,4R,5R,6aS)-4-((E)-4,4-difluoro-3-oxo-1-octenyI)-2-oxo-5-(phenylmethoxy)hexahydro-2H-cyclopenta[b]furan
https://huagongshe.com/reaction/1049954
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl (3,3-difluoro-2-oxoheptyl)phosphonate | HCID 11118722 | — |
| Reactant | (3aR,4R,5R,6aS)-hexahydro-2-oxo-5-(phenylmethoxy)-2H-cyclopenta[b]furan-4-carboxaldehyde | HCID 14460245 | — |
| Catalyst | HCID 178526214 | HCID 178526214 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | water MeOtBu | HCID 23212559 | — |
| Product | (3aR,4R,5R,6aS)-4-((E)-4,4-difluoro-3-oxo-1-octenyI)-2-oxo-5-(phenylmethoxy)hexahydro-2H-cyclopenta[b]furan | HCID 46862980 | 76% |
Reaction Steps
To a mixture of dimethyl(3,3-difluoro-2-oxoheptyl)phosphonate (210 mg, 0.81 mmoL) in MTBE/H2O (3/0.1 mL) was added Zn(OH)2 (100 mg, 0.81 mmoL) and the mixture was stirred under nitrogen for 1 h. A solution of (3aR,4R,5R,6aS)-hexahydro-2-oxo-5-(phenylmethoxy)-2H-cyclopenta[b]furan-4-carboxaldehyde (200 mg, 0.77 mmoL) in dichloromethane (3 mL) was added and the mixture was stirred for 24 h. After completion of the reaction, the reaction was then quenched with cold 1N HCl (12 mL). The organic layer was separated, washed with brine, dried over Na2SO4 and concentrated to dryness under vacuum. The crude material was further purified by column chromatography [25% ethyl acetate in heptanes] to yield (3aR,4R,5R,6aS)-4-((E)-4,4-difluoro-3-oxo-1-octenyl)-2-oxo-5-(phenylmethoxy)hexahydro-2H-cyclopenta[b]furan (7, R1 is phenyl, and R2 and R3 are H) in 76% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382272B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-51124c6f60614eacb08edd621d6248dc |
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| Source note | uspto-grants-2016_07 |
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