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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561730Generated: October 31, 2026

(3aR,4R,5R,6aS)-2-oxo-4-((E)-3-oxo-4-phenoxybut-1-en-1-yl)hexahydro-2H-cyclopenta[b]furan-5-yl benzoate → (3aR,4R,5R,6aS)-2-oxo-4-(3-oxo-4-phenoxybutyl)hexahydro-2H-cyclopenta[b]furan-5-yl benzoate

https://huagongshe.com/reaction/561730

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3aR,4R,5R,6aS)-2-oxo-4-((E)-3-oxo-4-phenoxybut-1-en-1-yl)hexahydro-2H-cyclopenta[b]furan-5-yl benzoateHCID 12767308—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product(3aR,4R,5R,6aS)-2-oxo-4-(3-oxo-4-phenoxybutyl)hexahydro-2H-cyclopenta[b]furan-5-yl benzoateHCID 22803341—

Reaction Steps

(3aR,4R,5R,6aS)-2-Oxo-4-((E)-3-oxo-4-phenoxybut-1-enyl)hexahydro-2H-cyclopenta[b]furan-5-yl benzoate, prepared in Step A, is dissolved in ethyl acetate and 10% Pd/C is added to the solution under a nitrogen atmosphere. The solution is flushed with hydrogen gas and subsequently stirred under a hydrogen atmosphere until starting material is consumed as judged by TLC. The crude reaction mixture is filtered through Celite and the solvent is removed under reduced pressure. The crude product is purified by flash chromatography on regular silica gel eluted with ethyl acetate-hexanes to afford the title intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063240B2
Source datasetuspto-grants-2011_11
ORD IDord-0b71dab0d80d4b7486fd74e21f3b39ee
Source noteuspto-grants-2011_11