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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058094Generated: November 1, 2026

Ethyl nipecotate → (R)-(-)-Ethyl Nipecotate Tartrate

https://huagongshe.com/reaction/1058094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl nipecotateHCID 98969—
ReactantL-Tartaric acidHCID 444305—
Reactant(R)-(-)-ethyl nipecotate L-(+)-tartrateHCID 86758823—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product(R)-(-)-Ethyl Nipecotate TartrateHCID 273369572%

Reaction Conditions

Temperature62.5 °C

Reaction Steps

L-(+)-Tartaric acid (47.74 g, 318 mmol) was suspended in 265 g of isopropyl alcohol and 16.91 g of water. The mixture was heated to 60-65° C. to afford a homogeneous solution. One equivalent of (±)-ethyl nipecotate (50 g, 318 mmol) was added while the temperature was maintained at or below 75° C. The mixture was stirred at 70-75° C. for 20-30 minutes, then cooled to 60° C. over 60 minutes. Seed crystals of (R)-(−)-ethyl nipecotate-L-(+)-tartrate (25 mg, 0.08 mmol) were added and the reaction was cooled to 26-30° C. over three hours. The temperature was maintained at 26-30° C. for 30 minutes until precipitation was complete. The product was isolated (62.0 g, 94.8% de) and washed twice with a mixture of isopropyl alcohol (21.05 g) and water (1.34 g). The crude product was slurried in a mixture of isopropyl alcohol (188 g) and water (12 g) at 73-77° C. After stirring for 10-20 minutes, the suspension was cooled to 26-30° C. Temperatures exceeding 30° C. will result in less yield, while a temperature of less than 25° C. resulted in de<98%. The product was isolated by filtration and washed twice with a mixture of isopropyl alcohol (21.05 g) and water (1.34 g). This afforded the title compound as a white powder in 72% yield, 98.8% de.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515130B1
Source datasetuspto-grants-2003_02
ORD IDord-fe05e1da699444369549defde138d795
Source noteuspto-grants-2003_02