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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941571Generated: November 2, 2026

Triethylamine → (2S,4R)-2-Methyl 1-(4-nitrobenzyl) 4-((methylsulfonyl)oxy)pyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/1941571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(2S, 4R)-4-hydroxy-N-(4-nitrobenzyloxycarbonyl)proline methyl esterHCID 18656014—
SolventDichloromethaneHCID 6344—
Product(2S,4R)-2-Methyl 1-(4-nitrobenzyl) 4-((methylsulfonyl)oxy)pyrrolidine-1,2-dicarboxylateHCID 57030081—

Reaction Steps

To a solution of (2S,4R)-1-p-nitrobenzyloxycarbonyl-4-hydroxypyrrolidine-2-carboxylic acid methyl ester (59.44 g: 0.183 mole) in dichloromethane (150 ml) stirring at -20° C., triethylamine (30.5 ml: 1.2 eq.) and methanesulfonyl chloride (17 ml: 1 eq.) are added. The mixture is stirred at the same temperature for 35 minutes. To the mixture is added ice water and ethyl acetate. The organic layer is taken, washed with water, dried over magnesium sulfate, and concentrated in vacuo to give (2S,4R)-1-p-nitrobenzyloxycarbonyl-4-methanesulfonyloxypyrrolidine-2-carboxylic acid methyl ester (74.05 g). Yield: Quantitative.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703243
Source datasetuspto-grants-1997_12
ORD IDord-e37b99d5eb3649e7928e090e92a7e18f
Source noteuspto-grants-1997_12