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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396869Generated: November 2, 2026

Iodo benzene diacetate → (5S)-1-{[(1,1-dimethylethyl)oxy]carbonyl}-4,5-dihydro-1H-pyrazole-5-carboxylic acid

https://huagongshe.com/reaction/1396869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodo benzene diacetateHCID 12217721—
Reactant(S)-2-(tert-Butoxycarbonyl)pyrazolidine-3-carboxylic acidHCID 58501748—
SolventMethanolHCID 887—
Product(5S)-1-{[(1,1-dimethylethyl)oxy]carbonyl}-4,5-dihydro-1H-pyrazole-5-carboxylic acidHCID 6828795964%

Reaction Steps

To a 50 ml round bottom flask was added (3S)-2-{[(1,1-dimethylethyl)oxy]carbonyl}-3-pyrazolidinecarboxylic acid (431 mg, 1.99 mmol) in methanol (15 mL), followed by iodobenzene diacetate (770 mg, 2.39 mmol). The mixture was stirred at room temperature for 10 min, and LCMS indicated the reaction was complete. The organic solvent was removed under vacuum, and the residue was taken up in 1 M aq. NaHCO3 (30 mL). The aqueous mixture was washed with DCM (3×20 mL), acidified with 6 N HCl to ˜pH 2.0, and then extracted with DCM (3×30 mL). The combined organic extracts were dried (Na2SO4), filtered, and concentrated under vacuum to afford (5S)-1-{[(1,1-dimethylethyl)oxy]carbonyl}-4,5-dihydro-1H-pyrazole-5-carboxylic acid (273 mg, 1.27 mmol, 64% yield) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-40e4be92484a4e949eaa4f64f196ad08
Source noteuspto-grants-2014_12