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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230516Generated: November 1, 2026

2-(3-Phenylpyrrolidin-3-yl)ethanol → (-)-3-phenyl-3-(2-hydroxyethyl)pyrrolidine (R,R)-di-p-anisoyltartaric acid

https://huagongshe.com/reaction/2230516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Phenylpyrrolidin-3-yl)ethanolHCID 18464564—
Reactant(R, R)-di-p-anisoyltartaric acidHCID 66875417—
SolventEthanolHCID 702—
Product(-)-3-phenyl-3-(2-hydroxyethyl)pyrrolidine (R,R)-di-p-anisoyltartaric acidHCID 7010970439.1%

Reaction Steps

Combine 3-phenyl-3-(2-hydroxyethyl)pyrrolidine (99.2 g, 659 mmol) and ethanol (2.5 L). Heat to reflux. Add a refluxing solution of (R,R)-di-p-anisoyltartaric acid (212 g, 507 mmol) in ethanol (5.07 L). After the addition is complete, slowly cool to ambient temperature with stirring to give an oil. Dissolve the oil in ethanol at reflux (595 mL) and add a refluxing solution of (R,R)-di-p-anisoyltartaric acid (49.2 g) in ethanol (1.1 L). Cool to ambient temperature with stirring to give a solid. Collect the solid by filtration and recrystallize from ethanol (3.2 L) to give a second solid. Collect the second solid by filtration and recrystallize from ethanol (2.6 L), seed with (−)-3-phenyl-3-(2-hydroxyethyl)pyrrolidine (R,R)-di-p-anisoyltartaric acid salt to give (−)-3-phenyl-3-(2-hydroxyethyl)pyrrolidine (R,R)-di-p-anisoyltartaric acid salt (121 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423704B1
Source datasetuspto-grants-2002_07
ORD IDord-93124c78f3d84e50aed26fc20b4cfc8d
Source noteuspto-grants-2002_07