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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1067100Erstellt: 26. Oktober 2026

Benzaldehyde → Nalpha-Benzyl-Ndelta-Boc-Ornithine

https://huagongshe.com/reaction/1067100

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktSodium HydroxideHCID 14798—
EduktSodium borohydrideHCID 4311764—
Edukt(2S)-2-amino-5-(((tert-butoxy)carbonyl)amino)pentanoic acidHCID 6993436—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
ProduktNalpha-Benzyl-Ndelta-Boc-OrnithineHCID 101104055—

Reaktionsschritte

A solution of Nδ-Boc-ornithine (7.0 g), 2M sodium hydroxide (20 ml), benzaldehyde (3.2 ml) and methanol (10 ml) was cooled to 0° C. and sodium borohydride (2.7 g) was added. After 1 hr at 0° C., the mixture was kept at 25° C. for 12 h. Water (100 ml) was added and the mixture extracted with ether (2×60 ml). The combined organic extract was washed with sat. sodium bicarbonate (ca. 150 ml) and water, and dried over anhydrous sodium sulfate. After concentration in vacuo, the desired product (4.5 g) was obtained as a white solid: 1H NMR (400 MHz, CD3OD) δ1.42 (s, 9H), 1.60 (m, 2H), 1.84 (m, 2H), 3.03 (m, 2H), 3.50 (t, J=7.4 Hz, 1H), 4.11 (d, J=11.9 Hz, 1H), 4.21 (d, J=11.9 Hz, 1H), 7.41 (m, 3H), and 7.49 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06245746B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-4a3a99e99369426c9f31187f82c89fa7
Quellennotizuspto-grants-2001_06