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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966018Generated: October 30, 2026

Dimethyl Sulfoxide → 3-[(3,4-Dichlorophenyl)-(4-fluorophenyl)amino]pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1966018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 3-(tosyloxy)pyrrolidine-1-carboxylateHCID 13591085—
Reactant(3,4-Dichlorophenyl)-(4-fluorophenyl)amineHCID 66657269—
SolventEthyl AcetateHCID 8857—
Product3-[(3,4-Dichlorophenyl)-(4-fluorophenyl)amino]pyrrolidine-1-carboxylic acid tert-butyl esterHCID 6665723517.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium hydride (0.19 g, 60% in oil) was added to 10 ml of dimethyl sulfoxide (DMSO) and stirred at 60° C. for one hour. Subsequently, 1.0 g of (3,4-dichlorophenyl)-(4-fluorophenyl)amine was added to the mixture and stirred at 60° C. for one hour. A DMSO solution containing 2.0 g of 3-(toluene-4-sulfonyloxy)pyrrolidine-1-carboxylic acid tert-butyl ester was gradually added to the mixture and stirred at 60° C. for 15 hours. Ethyl acetate was added to the reaction solution. The solution was then washed with water, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=20:1). The eluent solvent was distilled off under reduced pressure to thereby obtain 0.29 g of oily brown 3-[(3,4-dichlorophenyl)-(4-fluorophenyl)amino]pyrrolidine-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420623B2
Source datasetuspto-grants-2013_04
ORD IDord-d4efd9e4f57a49169370faef18479309
Source noteuspto-grants-2013_04