Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Tartaric acid | HCID 444305 | — |
| Reactant | (3R)-3-Aminopyrrolidine D(-)-tartrate | HCID 15107948 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86744075 | HCID 86744075 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04939256 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-9cc23bca007f479195bf8c3c05eb2e12 |
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| Source note | uspto-grants-1990_07 |
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