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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081546Generated: October 26, 2026

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

https://huagongshe.com/reaction/1081546

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 numberUS05587161
Source datasetuspto-grants-1996_12
ORD IDord-c07ce1fd132f4fee9e663cb7a93c11da
Source noteuspto-grants-1996_12