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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396893Generated: October 27, 2026

Sodium cyanoborohydride → Di-tert-butyl pyrazolidine-1,5-dicarboxylate

https://huagongshe.com/reaction/1396893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantDi-tert-butyl 4,5-dihydropyrazole-1,5-dicarboxylateHCID 68288059—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
ProductDi-tert-butyl pyrazolidine-1,5-dicarboxylateHCID 68287714100%

Reaction Conditions

Temperature25 °C

Reaction Steps

Di-tert-butyl 4,5-dihydropyrazole-1,5-dicarboxylate (12.65 g, 46.8 mmol) was dissolved in acetic acid (69.2 ml), and the solution was cooled in a water bath. Sodium cyanoborohydride (5.88 g, 94 mmol) was added portionwise under N2. The reaction was stirred at 25° C. for 5 hrs. The solvent was then removed under reduced pressure to give a residue. The residue was diluted with EtOAc (150 mL), and Na2CO3 (sat.) (100 mL) was cautiously added to the solution. The layers were separated and the aq. solution was extracted with EtOAc (2×30 mL), and the organics were dried over Na2SO4. The solvent was removed under reduced pressure to give the crude product di-tert-butyl pyrazolidine-1,5-dicarboxylate (12.74 g) as light yellow oil, which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-eb839b347516478685363a364736085e
Source noteuspto-grants-2014_12