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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906217Generated: October 25, 2026

Water → (2R,4S)-4-Acetoxy-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/906217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium AcetateHCID 517044—
Reactant(2R,4R)-1-(Toluene-4-sulfonyl)-4-(toluene-4-sulfonyloxy)-pyrrolidine-2-carboxylic Acid Ethyl EsterHCID 14541195—
SolventDimethylformamideHCID 6228—
Product(2R,4S)-4-Acetoxy-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic Acid Ethyl EsterHCID 15629284—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 1-(toluene-4-sulfonyl)-4-(toluene-4-sulfonyloxy)-pyrrolidine-2-carboxylic acid ethyl ester (2) (1 g, 2.14 mmol) in dry DMF (25 mL) is added potassium acetate (0.314 g, 3.21 mmol) in one portion. The reaction mixture is then heated at 60° C. for 4 h. Water (50 mL) is added to the reaction mixture and extracted with ethyl acetate (2×75 mL), combined organic layer are washed with water (2×50 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to give the crude compound. Crude compound is purified by column chromatography over silica gel (100-200 mesh) using 15% ethyl acetate-hexane as eluent to give compound (3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012983B2
Source datasetuspto-grants-2011_09
ORD IDord-9e2f7a1d3fd6492999db3178fcc2497d
Source noteuspto-grants-2011_09