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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081547Generated: October 25, 2026

di t-butyl 4-nitrobenzylcarbonyl-L-glutamate → di t-butyl 4-aminobenzylcarbonyl-L-glutamate

https://huagongshe.com/reaction/1081547

Reaction equation

Participants

RoleNameHCIDCharge
Reactantdi t-butyl 4-nitrobenzylcarbonyl-L-glutamateHCID 86748613—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Productdi t-butyl 4-aminobenzylcarbonyl-L-glutamateHCID 86748612—

Reaction Steps

A solution of di t-butyl 4-nitrobenzylcarbonyl-L-glutamate (9.7 g) in ethyl acetate (200 ml) was hydrogenated over 30% Pd/C (900 mg). The mixture was then filtered through Celite and evaporated to yield a yellow oil (di t-butyl 4-aminobenzylcarbonyl-L-glutamate) which was used without further purification. NMR: 8.23(d)1H; 6.92(d)2H; 6.50(d)2H; 4.86(s)2H; 4.15(m)1H; 3.24(s)2H; 2.22(m)2H; 1.8(m)2H); 1.4(d)18H. Yield 8.2 g 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587161
Source datasetuspto-grants-1996_12
ORD IDord-b6aefa24ee5445b4899ec130c5c74346
Source noteuspto-grants-1996_12