Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | D-Pyroglutamic acid | HCID 439685 | — |
| Produkt | ethyl (2R)-5-oxopyrrolidine-2-carboxylate | HCID 643508 | — |
Reaktionsschritte
To a solution of (R)-5-oxopyrrolidine-2-carboxylic acid (10 g, 69.84 mmol; available from Aldrich#422614) in EtOH (100 ml) cooled at −5° C., thionyl chloride (10 ml, 139.68 mmol) was added and the resulting mixture was stirred at RT for 3 hrs. Solvents were evaporated in vacuo and the resulting residue was taken up with EtOAc (350 ml), washed with water/TEA (40/12 ml), then with water (40 ml). Collected organics were dried over Na2SO4 and evaporated to afford a residue that was loaded on a SNAP-Si cartridge (50 g) and eluted with a mixture DCM/EtOAc from 90/10 to 50/50. Collected fractions after solvent evaporation afforded a first batch of title compound (D23) (6.4 g). The aqueous were saturated with NaCl and extracted with EtOAc (400 ml). The organic was washed with water (20 ml) dried over Na2SO4 and evaporated in vacuo to afford a second batch of title compound (D23) (3.7 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09181279B2 |
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| Quelldatensatz | uspto-grants-2015_11 |
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| ORD ID | ord-184e96fdbcb74c6c839564258576c07e |
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| Quellennotiz | uspto-grants-2015_11 |
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