Hydrochloric Acid → HCID 67408131, Verbindung
Reaktionsgleichung
C([O:5][C:6](=[O:18])[CH:7](C#N)[C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH3:15])=[CH:10][N:9]=1)(C)(C)C.Cl>O>[CH2:14]([C:11]1[CH:12]=[CH:13][C:8]([CH2:7][C:6]([OH:18])=[O:5])=[N:9][CH:10]=1)[CH3:15]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 104 °C
Versuchsvorschrift
Cyano-(5-ethyl-pyridin-2-yl)-acetic acid tert-butyl ester (7.3 g) was mixed with 70 mL of water and 70 mL of 12N HCl and was heated at 104° C. for 3 hours before removing the volatiles in vacuo. Water was added to dissolve the solids and the pH of the solution was adjusted to 9-10 with 2N NaOH. The solution was washed with 2-methylTHF (2×). The aqueous solution was adjusted to pH 4 with 2N HCl and was concentrated under vacuum to an oily solid. The residue was triturated with hot chloroform and heptanes to afford (5-ethylpyridin-2-yl)acetic acid (SM-1ac) as a tan solid (3.88 g, 31%, 3 steps). MS (ES+) 166.1 (M+H)+. 1H NMR (DMSO-d6) δ 1.16 (t, 3H), 2.57 (q, 2H), 3.66 (s, 2H), 7.22 (d, 1H), 7.56 (dd, 1H), 8.31 (d, 1H), 12.44 (br s, 1H).