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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157724Generated: October 26, 2026

Ethanol → 3-(2-(R)-Methyl-pyrrolidin-1-yl)-propionic acid ethyl ester

https://huagongshe.com/reaction/1157724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl AcrylateHCID 8821—
ReactantPotassium CarbonateHCID 11430—
Reactant(2R)-(-)-2-Methylpyrrolidine hydrochlorideHCID 11147704—
SolventAcetonitrileHCID 6342—
Product3-(2-(R)-Methyl-pyrrolidin-1-yl)-propionic acid ethyl esterHCID 59696738100.8%

Reaction Steps

In a round-bottom flask, 2-(R)-methylpyrrolidine HCl (5.5 g, 45 mmol) was dissolved in CH3CN (20 mL). To the stirred solution was added milled K2CO3 (8.3 g, 60 mmol). The suspension was stirred at room temperature for approximately 1 h. Ethyl acrylate (3.25 mL, 30 mmol) and EtOH (40 mL) were then added. The reaction mixture was stirred until analysis by GC showed completion (the Area % of ethyl acrylate was less than 1% (approximately 2 h)). The reaction mixture was filtered and the wet cake (excess K2CO3) was washed with CH3CN (5-10 mL). The filtered solution was then concentrated under reduced pressure to minimum volume (white slurry). Methyl t-butyl ether (MTBE) and H2O were added, at which time all solids dissolved. The organic layer was washed a second time with water and then concentrated to yield 5.6 g of the title compound. The oil product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807697B2
Source datasetuspto-grants-2010_10
ORD IDord-1813f9df006f4e28bf5b776794cdcedd
Source noteuspto-grants-2010_10