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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185497Generated: November 3, 2026

Dimethyl Sulfoxide → (2s,4r)-n-Tert-butoxycarbonyl-4-(n-tert-butoxycarbonylglycylamino)-2-pyrrolidinecarboxaldehyde

https://huagongshe.com/reaction/2185497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(2s,4r)-4-(n-Tert-butoxycarbonylglycylamino)-2-hydroxymethyl-n-tert-butoxycarbonylpyrrolidineHCID 70172939—
SolventDichloromethaneHCID 6344—
Product(2s,4r)-n-Tert-butoxycarbonyl-4-(n-tert-butoxycarbonylglycylamino)-2-pyrrolidinecarboxaldehydeHCID 7394749197.9%

Reaction Steps

The following reaction was carried under argon. Dimethyl sulfoxide (288 μL) was added to a stirred solution of oxalyl chloride (177 mL) in dichloromethane (3 mL) at −78° C. After stirring at the same temperature for 15 min, a solution of (2S,4R)-N-tert-butoxycarbonyl-4-(N-tert-butoxycarbonylglycylamino)-2-hydroxymethylpyrrolidine (151 mg) in dichloromethane (3 mL) was added. The mixture was stirred at −78° C. for 2 hr, and triethylamine (848 μL) was added to the reaction mixture. The mixture was stirred at 0° C. for 1 hr, quenched with saturated ammonium chloride, and extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate and evaporated in vacuo. The residue was purified by silica gel column chromatography (chloroform then chloroform:methanol=99:1 to 97:3, v/v) to give the titled compound (147 mg) as a colorless foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399629B1
Source datasetuspto-grants-2002_06
ORD IDord-03fc29335e094994a8fa838f145795ca
Source noteuspto-grants-2002_06