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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300802Generated: November 1, 2026

Dimethyl Sulfoxide → Benzyl 2-formylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/2300802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 69961783HCID 69961783—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductBenzyl 2-formylpyrrolidine-1-carboxylateHCID 11064320—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 10 mL CH2Cl2 and 2.1 mL oxalyl chloride at −78° C. was added a solution of DMSO (1.04 mL) in CH2Cl2 (3 mL) dropwise over 10 min while stirring. After the mixture was stirred for 10 min, a solution of the (S)-(+)-1-benzyloxycarboxy-2-pyrrolidinemethanol (1.5 g) in CH2Cl2 (4 mL) was added slowly over 10 min. The reaction mixture was then stirred at −78° C. for 1.5 h followed by the addition of 4.46 mL triethylamine. After stirring at −78° C. for 30 min, the mixture was warmed up to 0° C. and then stirred for 20 min at 0° C. To the mixture was added 1 mL of MeOH followed by addition of 8 mL of water. The aquous layer was separated and extracted with CH2Cl2 (3×60 mL). The combined organic layer was washed with NaHCO3, H2O and brine, successively, and dried (Na2SO4). Removal of the solvent provided 1.5 g of the title compound which was used directly for next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498165B1
Source datasetuspto-grants-2002_12
ORD IDord-e0aeb20d402f4980ab0fa4fe3526ba36
Source noteuspto-grants-2002_12