Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl (3,3-difluoro-2-oxoheptyl)phosphonateHCID 11118722—
Reactant(3aR,4R,5R,6aS)-hexahydro-2-oxo-5-(phenylmethoxy)-2H-cyclopenta[b]furan-4-carboxaldehydeHCID 14460245—
CatalystHCID 178526214HCID 178526214—
SolventDichloromethaneHCID 6344—
Solventwater MeOtBuHCID 23212559—
Product(3aR,4R,5R,6aS)-4-((E)-4,4-difluoro-3-oxo-1-octenyI)-2-oxo-5-(phenylmethoxy)hexahydro-2H-cyclopenta[b]furanHCID 4686298076%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382272B2
Source datasetuspto-grants-2016_07
ORD IDord-51124c6f60614eacb08edd621d6248dc
Source noteuspto-grants-2016_07