Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861217Generated: October 25, 2026

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

https://huagongshe.com/reaction/861217

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Nitrophenyl)acetic acidHCID 4661—
ReactantDimethylformamideHCID 6228—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantL-Glutamic acid di-tert-butyl esterHCID 208637—
Productdi t-butyl 4-nitrobenzylcarbonyl-L-glutamateHCID 8674861377%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05714148
Source datasetuspto-grants-1998_02
ORD IDord-796d4fcfc51c40ed8eb9649c8cc9f03d
Source noteuspto-grants-1998_02