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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470680Generated: November 4, 2026

TBS-COREY LACTONE ALDEHYDE → HCID 68733852, compound

https://huagongshe.com/reaction/1470680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTBS-COREY LACTONE ALDEHYDEHCID 10989745—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86630288HCID 86630288—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68733852HCID 6873385291.2%

Reaction Steps

n-heptylphosphonium bromide (3.185 g, 7.22 mmol) was dried under vacuum for 3 days and was then taken into dry THF (22 mL). Potassium tert-butoxide (7.2 mL, 7.2 mmol, 1 M/THF) was added and the resulting red-orange solution was stirred for 45 min. at room temperature. A solution of (3aR,4R,5R,6aS)-5-(tert-butyldimethylsilyloxy)-2-oxohexahydro-2H-cyclopenta[b]furan-4-carbaldehyde (5-1, 502 mg, 1.78 mmol, Cayman) in 7 mL THF was added by cannula, rinsing with 3 mL THF. After 1.5 h, the reaction was quenched by addition of saturated NH4Cl solution. The resulting mixture was extracted with ethyl acetate (3×) and the combined ethyl acetate solution was dried (Na2SO4), filtered and evaporated. Purification of the residue by flash chromatography on silica gel (Isco Combiflash unit) gave the title compound (595 mg, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006464B2
Source datasetuspto-grants-2015_04
ORD IDord-2c611dcaa9524007ad009d5888c9284f
Source noteuspto-grants-2015_04