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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1267856Erstellt: 26. Oktober 2026

Benzyl chloroformate → (2S)-2-{[(benzyloxy)carbonyl]amino}-2-methylpentanedioic acid

https://huagongshe.com/reaction/1267856

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl chloroformateHCID 10387—
Edukt2-Methylglutamic acidHCID 95440—
LösungsmittelSodium HydroxideHCID 14798—
Produkt(2S)-2-{[(benzyloxy)carbonyl]amino}-2-methylpentanedioic acidHCID 2068120583%

Reaktionsschritte

To a stirred solution of α-methyl-D,L-glutamic acid (10 g, 62 mmol) in 2 N sodium hydroxide (62 mL) at 0.5° C. was added benzyl chloroformate (12.7 g, 74.4 mmol) over 30 min. After the addition was complete the reaction mixture was stirred at room temperature for 3 hours. During, this time the pH was maintained at 11 by addition of 2N sodium hydroxide (33 mL). The reaction mixture was then extracted with ether (60 mL). The aqueous layer was cooled in an ice bath and then acidified with 4N hydrochloric acid (34 mL) to pH=1. The resulting mixture was extracted with ethyl acetate (3×100 mL). The combined ethyl acetate extracts were washed with brine (60 mL) and dried (MgSO4). The solvent was removed in vacuo to give 15.2 g (83%) of N-benzyloxycarbonyl-α-methylglutamic acid as an oil: 1H NMR (CDCl3) δ 8.73(m, 5H), 5.77(b, 1H), 5.09(s, 2H), 2.45-2.27(m, 4H), 2.0(s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06555554B2
Quelldatensatzuspto-grants-2003_04
ORD IDord-1467c5a528f1437a9ac43defa4ba8421
Quellennotizuspto-grants-2003_04