Tetrahydrofuran → (s)-2-(2-Oxo-2h-pyridin-yl)-propionic acid

A stirred mixture of (S)-2-(2-Oxo-2H-pyrid-1-yl)-propionic acid ethyl ester (364 mg, 1.87 mmol), THF (2 ml), water (1 ml) and sodium hydroxide (90 mg, 2.24 mmol) was kept at room temperature for 1 h, then concentrated under reduced pressure. The residue was dissolved in ether and the resulting solution washed with water. The organic layer was discarded and the aqeous layer was acidified with concentrated HCl then extracted several times with ethyl acetate. The combined organic extracts were dried (MgSO4), filtered and concentrated. The residue was triturated with ether to afford the title compound as a colorless solid (84 mg, 27%): [α]31D=−50° (c=0.2, CH3OH) 1H NMR (400 MHz, DMSO) δ 1.5 3H, d), 5.1 1H, q), 6.2 1H, t), 6.4 1H, d), 7.4 1H, m), 7.6 1H, d).

1. concentrationconcentrated under reduced pressure
2. dissolutionThe residue was dissolved in ether
3. washthe resulting solution washed with water
4. extractionthen extracted several times with ethyl acetate
5. dry with materialThe combined organic extracts were dried (MgSO4)
6. filtrationfiltered
7. concentrationconcentrated
8. customThe residue was triturated with ether

ORD record

ord-061779ebb49a420ebef5adb91cbcc75c

Source dataset

uspto-grants-2009_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07517987B2