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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9942Generated: October 26, 2026

Triethylamine → Methyl (2S,4R)-4-methylsulfonyloxy-1-methyl-2-pyrrolidinecarboxylate

https://huagongshe.com/reaction/9942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl (2S,4R)-4-hydroxy-1-methyl-2-pyrrolidinecarboxylate hydrochlorideHCID 86590358—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl (2S,4R)-4-methylsulfonyloxy-1-methyl-2-pyrrolidinecarboxylateHCID 1208250383%

Reaction Conditions

Temperature40 °C

Reaction Steps

Triethylamine (1.53 mL) was added to a suspension of methyl (2S, 4R)-4-hydroxy-1-methyl-2-pyrrolidinecarboxylate hydrochloride (1 g) obtained from Reference example 1 or 3 in tetrahydrofuran (10 mL) and the mixture was stirred at 40° C. for 3 hours. Mesyl chloride was added to the mixture under ice cooling and the mixture was stirred for 2 hours. Ethyl acetate (20 mL) and 5% aqueous sodium hydrogencarbonate solution (10 mL) were added to the reaction mixture, which was then extracted. The organic layer was separated from the aqueous layer and the solvent of the organic layer was removed by distillation under reduced pressure to give the title compound (1.0 g, yield 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091363B2
Source datasetuspto-grants-2006_08
ORD IDord-1588a0231fd14c6f8e892efabb879249
Source noteuspto-grants-2006_08