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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240230Generated: October 27, 2026

Dicyclohexylcarbodiimide → 2,5-dioxopyrrolidin-1-yl(S)-3-(3,5-dinitrobenzamido)-3-phenylpropionate

https://huagongshe.com/reaction/240230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant(S)-3-(3,5-dinitrobenzamido)-3-phenylpropionic acidHCID 44255973—
SolventTetrahydrofuranHCID 8028—
Product2,5-dioxopyrrolidin-1-yl(S)-3-(3,5-dinitrobenzamido)-3-phenylpropionateHCID 86634315—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

12 g of (S)-3-(3,5-dinitrobenzamido)-3-phenylpropionic acid from reaction b) were dissolved in 120 ml of tetrahydrofuran and admixed with 3.92 g of N-hydroxysuccinimide. With cooling in an icebath at 0-5° C., 7.1 g of dicyclohexylcarbodiimide was added in portions to the reaction mixture. On completion of addition, the mixture was left in the icebath with further stirring until the solution reached room temperature. After the reaction ended (HPLC monitoring >95 area % conversion), the precipitated dicyclohexylurea was filtered off and washed with tetrahydrofuran. The filtrate was concentrated under reduced pressure, and the residue digested at reflux in 250 ml of 2-propanol for 2 h. The product was filtered off with suction, washed with 2-propanol and dried at 50° C. under reduced pressure. The yield was 13.87 g; HPLC purity 98.8 area %.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08647882B2
Source datasetuspto-grants-2014_02
ORD IDord-cfb75f8d5e244d69bcebab391471214f
Source noteuspto-grants-2014_02