Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073317Generated: November 2, 2026

L-Tartaric acid → HCID 86744075, compound

https://huagongshe.com/reaction/1073317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Tartaric acidHCID 444305—
Reactant(3R)-3-Aminopyrrolidine D(-)-tartrateHCID 15107948—
SolventWaterHCID 962—
ProductHCID 86744075HCID 86744075—

Reaction Conditions

Temperature80 °C

Reaction Steps

To the filtrate obtained in the above crude (3R)-3-aminopyrrolidine D(-)-tartrate is added a solution of L(+)-tartaric acid (25 g) in water (50 ml), and the precipitated crystals are separated by filtration. The product is dissolved in a 20% aqueous sodium hydroxide solution (50 ml) and thereto is added acetone (300 ml), and the precipitated crystals are removed by filtration. To the filtrate is added a solution of L(+)-tartaric acid (20 g) in water (40 ml). The precipitated crystals are separated by filtration and dissolved in water (30 ml), and thereto is added sodium hydroxide (300 g). The mixture is extracted with ether (300 ml) three times. Ether is distilled off under reduced pressure, and to the residue is added a solution of L(+)-tartaric acid (5.5 g) in water (25 ml), and the mixture is heated at 80° C. To the mixture is added methanol (40 ml), and the mixture is gradually cooled till room temperature. The precipitated crystals are separated by filtration and recrystallized from a mixed solvent of methanol-water (1:1) to give (3S)-3-aminopyrrolidine L(+)tartrate (5.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968800
Source datasetuspto-grants-1990_11
ORD IDord-547b994f032d4200a72ebb323c55d1b8
Source noteuspto-grants-1990_11