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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709183Generated: October 29, 2026

Hydrogen Peroxide → HCID 46181891, compound

https://huagongshe.com/reaction/709183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 67175633HCID 67175633—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 46181891HCID 4618189187%

Reaction Steps

To a mixture of ethyl 3-(5-(benzo[d][1,3]dioxol-5-yl)-1-(4-cyano-2-methylphenyl)-1H-pyrrol-2-yl)propanoate (100 mg, 0.249 mmol) and potassium carbonate (52 mg, 0.373 mmol) in DMSO (1 mL) was added 30% aqueous H2O2 (28.2 mg, 0.249 mmol). The resultant mixture was stirred at room temperature for 2 h. TLC showed the reaction was completed. Water (7 mL) was added and white solid precipitated. The suspension was centrifuged and the aqueous phase was discarded. The resultant solid was dried in vacuum to afford the amide intermediate as a white solid (85 mg, yield 81%). To the mixture of this intermediate in H2O (0.6 mL) and THF (0.6 mL) was added LiOH H2O (10 mg, 0.238 mmol). The reaction mixture was stirred at room temperature overnight. THF was evaporated in vacuum. The residue was acidified to pH=4 with 5% hydrochloric acid, centrifuged and dried to afford 3-(5-(benzo[d][1,3]dioxol-5-yl)-1-(4-carbamoyl-2-methylphenyl)-1H-pyrrol-2-yl)propanoic acid as a white solid (46 mg, overall yield 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09180119B2
Source datasetuspto-grants-2015_11
ORD IDord-e690b3552f1a46d8ae36220fd9344743
Source noteuspto-grants-2015_11