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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Reactant | (S)-2-(tert-Butoxycarbonyl)pyrazolidine-3-carboxylic acid | HCID 58501748 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5S)-1-{[(1,1-dimethylethyl)oxy]carbonyl}-4,5-dihydro-1H-pyrazole-5-carboxylic acid | HCID 68287959 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08901119B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-40e4be92484a4e949eaa4f64f196ad08 |
|---|
| Source note | uspto-grants-2014_12 |
|---|