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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408857Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 66657281, compound

https://huagongshe.com/reaction/2408857

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 numberUS08815871B2
Source datasetuspto-grants-2014_08
ORD IDord-30da6a30070b48a3ae3b8e07be5513f8
Source noteuspto-grants-2014_08