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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1081546Erstellt: 26. Oktober 2026

(4-Nitrophenyl)acetic acid → di t-butyl 4-nitrobenzylcarbonyl-L-glutamate

https://huagongshe.com/reaction/1081546

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(4-Nitrophenyl)acetic acidHCID 4661—
EduktDimethylformamideHCID 6228—
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktL-Glutamic acid di-tert-butyl esterHCID 208637—
Produktdi t-butyl 4-nitrobenzylcarbonyl-L-glutamateHCID 8674861377%

Reaktionsschritte

1-Hydroxybenzotriazole (4.05 g) was added to a solution of 4-nitrophenyl acetic acid (5.4 g) in dimethylformamide (75 ml). L-Glutamic acid di tert-butyl ester (7.77 g) and then dicyclohexylcarbodiimide (6.2 g) were added to the mixture. The mixture was then stirred for 18 hr at ambient temperature. The mixture was filtered and the filtrate washed with saturated sodium bicarbonate solution, water and 0.5 m hydrochloric acid and then dried and evaporated to dryness. The residue was chromatographed on silica gel by eluting with hexane/ethyl acetate (2:1) to give di t-butyl 4-nitrobenzylcarbonyl-L-glutamate as an oil 9.7 g (77%). NMR: 8.2(d)2H; 7.45(d)2H; 6.45(d)1H; 4.45(m)1H; 3.15(s)2H; 2.1(m)4H; 1.4(d)9H; 1.35(s)9H.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05587161
Quelldatensatzuspto-grants-1996_12
ORD IDord-c07ce1fd132f4fee9e663cb7a93c11da
Quellennotizuspto-grants-1996_12