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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404665Generated: October 25, 2026

Hydrochloric Acid → 2-(2-Oxopyrrolidin-1-yl)-2-phenylacetic acid

https://huagongshe.com/reaction/404665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-(4-Chlorobutanamido)-2-phenylacetic acidHCID 86688926—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Oxopyrrolidin-1-yl)-2-phenylacetic acidHCID 1325429663.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(4-Chlorobutanamido)-2-phenylacetic acid (650 mg, 2.54 mmol) was dissolved in dry THF (8.5 ml) and the solution was cooled to 0° C. with an ice-bath stirring under nitrogen atmosphere. Potassium tert-butoxide (599 mg, 5.34 mmol) was added in three portions and a white suspension was obtained. The mixture was stirred at the same temperature for 15 minutes. 1N HCl was added dropwise till pH 2-3 and than the mixture was diluted with water (10 ml) and extracted three times with EtOAc (15 ml×3). The organic phase was dried (Na2SO4) and evaporated to obtain the title compound (352 mg, 63.2% yield) as a pale yellow spongy sticky solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748613B2
Source datasetuspto-grants-2014_06
ORD IDord-40fc3a5568e54e078c00a86c71480509
Source noteuspto-grants-2014_06