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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966019Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 66657281, compound

https://huagongshe.com/reaction/1966019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
ReactantHCID 3027195HCID 3027195—
ReactantTert-butyl (3R)-3-(methanesulfonyloxy)pyrrolidine-1-carboxylateHCID 10934372—
SolventEthyl AcetateHCID 8857—
ProductHCID 66657281HCID 666572815.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium hydride (0.36 g, 60% in oil) was added to 20 ml of dimethyl sulfoxide (DMSO) and stirred at 60° C. for one hour. Subsequently, 2.0 g of 3,4-dichlorophenyl-phenylamine was added to the mixture and stirred at 60° C. for one hour. A DMSO solution containing 1.5 g of 3(R)-methanesulfonyloxypyrrolidine-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, and the reaction 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 0.13 g of light brown amorphous solid 3(S)-[(3,4-dichlorophenyl)phenylamino]pyrrolidine 1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420623B2
Source datasetuspto-grants-2013_04
ORD IDord-3de31812ea8c4caab07105e4824538ad
Source noteuspto-grants-2013_04