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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411749Generated: October 29, 2026

Dimethyl Sulfoxide → 1-tert-butyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/411749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
Reactant1-(tert-butyl) 2-methyl (2S)-4-hydroxypyrrolidine-1,2-dicarboxylateHCID 12185578—
SolventDichloromethaneHCID 6344—
Product1-tert-butyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylateHCID 1098848581.5%

Reaction Steps

A solution of 3.5 mL (40.2 mmol) of oxalyl chloride in 20 mL of CH2Cl2 was cooled in a −78° C. bath and 3.5 mL (49.3 mmol) of dry DMSO was added. After 30 min, a solution of 5.31 g (23 mmol) of N-(BOC)-4-hydroxy-(L)-proline, methyl ester was added. A precipitate developed during the addition. After 30 min at −78° C., 15 mL (107 mmol) of TEA was added. Another 30 mL of CH2Cl2 was added to the reaction mixture to facilitate stirring and cold bath was removed. After 1.5 hr the solution was partitioned between CH2Cl2 and water. The organic layer was washed with water, 1.2 N HCl, brine then dried over anydrous Na2SO4. The filtrate was concentrated in vacuo and the residue was purified by flash column chromatography on silica gel eluted with a gradient of 20-40% EtOAc/hexane to yield N-(BOC)-4-oxo-(L)-proline, methyl ester (4.56 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559174B2
Source datasetuspto-grants-2003_05
ORD IDord-38f0679520594e8eaf4db0b89236b21b
Source noteuspto-grants-2003_05