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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539936Generated: October 31, 2026

Dimethyl Sulfoxide → tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/539936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
Reactant(S)-(-)-N-Boc-prolinolHCID 643448—
SolventDichloromethaneHCID 6344—
Producttert-butyl (2S)-2-formylpyrrolidine-1-carboxylateHCID 2734674100.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 2 L, 3-necked round bottomed flask equipped with an overhead stir and a N2 inlet was charged with a solution of oxalyl chloride (130 mL, 0.26 mol) in DCM (250 mL). The solution was cooled to −78° C., and a solution of DMSO (20 mL, 0.28 mol) in DCM (30 mL) was added dropwise. After 30 minutes, a solution of (S)—N-Boc-prolinol (40 g, 0.20 mol) in DCM (200 mL) was added dropwise. After 30 minutes, TEA (140 mL, 1.00 mol) was added to the solution, and the flask was transferred to an ice/water bath and stirred for another 30 minutes. The reaction mixture was diluted with DCM (200 mL) and washed successively with H2O, 1M HCl, saturated NaHCO3, and brine. The DCM layer was dried over Na2SO4, filtered, and concentrated to afford crude (S)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (40 g) as an oil, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871759B2
Source datasetuspto-grants-2014_10
ORD IDord-081762726027441aa10603c8a0222690
Source noteuspto-grants-2014_10