HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011602Generated: October 30, 2026
Triacetoxyperiodinane → HCID 57659763, compound
https://huagongshe.com/reaction/1011602
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 67313638 | HCID 67313638 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57659763 | HCID 57659763 | 45% |
Reaction Steps
(2S,3R)-tert-Butyl 3-(tert-butyldimethylsilyloxy)-2,5-dicyclopropylpyrrolidine-1-carboxylate (19) (412 mg, 1.08 mmol) was dissolved in THF (1 mL) and placed under nitrogen. TBAF (IM THF, 1.29 mL) was added and the reaction stirred for 2 hr. The reaction was concentrated in vacuo and used without further purification. This material was dissolved in CH2Cl2 (2 mL) and placed under nitrogen. Dess-Martin reagent (788 mg, 1.86 mmol) was added and the reaction quenched with sat. aq. NaHCO3 (2 mL) followed by sat. Na2S2O3 (2 mL) when complete as indicated by TLC monitoring. The organic layer was isolated and concentrated in vacuo. The resulting crude product was purified by column chromatography using EtOAc/hexane gradients to yield (2S)-tert-butyl 2,5-dicyclopropyl-3-oxopyrrolidine-1-carboxylate (20) (128 mg, 45% over two steps) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977368B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-990422ac89654c95a68f6cf216b61795 |
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| Source note | uspto-grants-2011_07 |
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