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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011602Generated: October 30, 2026

Triacetoxyperiodinane → HCID 57659763, compound

https://huagongshe.com/reaction/1011602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 67313638HCID 67313638—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57659763HCID 5765976345%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977368B2
Source datasetuspto-grants-2011_07
ORD IDord-990422ac89654c95a68f6cf216b61795
Source noteuspto-grants-2011_07