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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | TBS-COREY LACTONE ALDEHYDE | HCID 10989745 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86630288 | HCID 86630288 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68733852 | HCID 68733852 | 91.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006464B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-2c611dcaa9524007ad009d5888c9284f |
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| Source note | uspto-grants-2015_04 |
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