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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269866Generated: October 30, 2026

Hydrochloric Acid → HCID 131723019, compound

https://huagongshe.com/reaction/2269866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-(3-Phenylpyrrolidin-3-yl)ethanolHCID 18464564—
Reactant(R, R)-di-p-anisoyltartaric acidHCID 66875417—
SolventMethanolHCID 887—
SolventMethanol--water (1/1)HCID 22242641—
ProductHCID 131723019HCID 131723019—

Reaction Steps

Combine (R, R)-di-p-anisoyltartaric acid (1.10 g, 2.62 mmol) in water/methanol (13.6 mL/13.6 mL). Add 12 M hydrochloric acid solution (0.217 mL, 2.63 mmol). Add a hot solution of 3-phenyl-3-(2-hydroxy-ethyl)-pyrrolidine (1.0 g, 5.23 mmol) in methanol (13.6 mL). Heat to reflux. After 30 minutes, slowly cool to ambient temperature to give a solid. Collect the solid by filtration and recrystallize the solid twice from methanol/water, once from methanol/2-butanone, and once from ethanol to give (+)-3-phenyl-3-(2-hydroxy-ethyl)-pyrrolidine (R, R)-di-p-anisoyltartaric acid-hydrochloric acid salt. After conversion of a sample to the 3,4,5-trimethoxybenzamide using sodium carbonate and 3,4,5-trimethoxybenzoyl chloride in acetone/water, analysis on HPLC using a CHIRALPAK AD (10 μm×4.6 cm×250 cm) column eluting with pentane/ethanol/methanol/triethylamine (80/15/5/0.1) with a flow rate of 1.5 mL/minute indicates an enantiomeric excess of 98%, (98% ee), retention time 22.30 minutes for the 3,4,5-trimethoxybenzamide of the (+)-isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329392B1
Source datasetuspto-grants-2001_12
ORD IDord-381811757c224e08ab6f3f311eacb299
Source noteuspto-grants-2001_12