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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412550Generated: October 31, 2026

Lithium Hydroxide → 4-(1-Tert-butoxycarbonylpyrrolidin-3-yloxy)phenoxyacetic acid

https://huagongshe.com/reaction/412550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactant4-(1-tert-Butoxycarbonylpyrrolidin-3-yloxy)phenoxyacetic acid ethyl esterHCID 60064215—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Tert-butoxycarbonylpyrrolidin-3-yloxy)phenoxyacetic acidHCID 1853634399.7%

Reaction Steps

To a solution of 4-(1-tert-butoxycarbonylpyrrolidin-3-yloxy)phenoxyacetic acid ethyl ester (2.5 g) in a mixture of tetrahydrofuran (5 ml) and ethanol (5 ml) was added 1N aqueous lithium hydroxide solution (7.5 ml) with ice-cooling, and the mixture was stirred at room temperature for 30 min. After completion of the reaction, the solvent was evaporated and to the obtained residue were added ice water and 10% aqueous citric acid solution, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was dried under reduced pressure to give the title compound(2.30 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562828B1
Source datasetuspto-grants-2003_05
ORD IDord-b66f0f746141458c9a594ff45484dda6
Source noteuspto-grants-2003_05