HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734225Generated: October 31, 2026
8-Azaspiro[4.5]dec-2-ene-7,9-dione → 8-Azaspiro[4.5]dec-2-ene
https://huagongshe.com/reaction/734225
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 8-Azaspiro[4.5]dec-2-ene-7,9-dione | HCID 15068034 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Azaspiro[4.5]dec-2-ene | HCID 22341335 | 99.8% |
Reaction Steps
To a solution of 8-azaspiro[4.5]dec-2-ene-7,9-dione (3.3 g, 20 mmol) [prepared according to Cipollina, J. A.; et. al. J. Med. Chem. 1991, 34, 3316.] in THF (200 mL) at 0° C. was added LAH (3.42 mg, 90 mmol) portion-wise. After 1 h at 0° C., the solution warmed to 25° C. and was then heated to 60° C. After an additional 1 h at reflux, the solution was cooled and quenched by dropwise addition of a saturated solution of Rochelle's salt. The aqueous phase was extracted several times with DCM and the combined organic fractions were dried (Na2SO4), concentrated and purified via column chromatography (silica, 3% MeOH in DCM (1% NH4OH)) yielding the title compound (2.74 g, quant.) as a yellow oil: LCMS (ES) m/e 160 (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592334B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-f1ad9c64806940ac9c9207dcecffc0b4 |
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| Source note | uspto-grants-2009_09 |
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