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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13777Generated: October 31, 2026

Water → (2R,4R)-tert-butyl 2-methyl-4-(tosyloxy)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/13777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant114676-93-6HCID 14117010—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product(2R,4R)-tert-butyl 2-methyl-4-(tosyloxy)pyrrolidine-1-carboxylateHCID 8661272385.5%

Reaction Steps

To a solution of 1.02 g of (2R,4R)-1-(t-butoxycarbonyl)-4-hydroxy-2-methylpyrrolidine (J. Med. Chem., 1988, 31, 1598-1611) in 10 ml of anhydrous dichloromethane, 1.7 ml of triethylamine and 1.16 g of p-toluenesulfonyl chloride were added, and then the mixture was stirred at room temperature overnight. The reaction solution was mixed with water, and followed by extraction with ethyl acetate twice. The organic layers were combined, washed in turn with water, 1N hydrochloric acid and a 1N aqueous sodium hydroxide solution and dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 1.54 g of the objective compound as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728131B2
Source datasetuspto-grants-2010_06
ORD IDord-7dea641aca3c49829f4b05f3cf36b2e6
Source noteuspto-grants-2010_06