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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | (S)-3-(3,5-dinitrobenzamido)-3-phenylpropionic acid | HCID 44255973 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,5-dioxopyrrolidin-1-yl(S)-3-(3,5-dinitrobenzamido)-3-phenylpropionate | HCID 86634315 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08647882B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-cfb75f8d5e244d69bcebab391471214f |
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| Source note | uspto-grants-2014_02 |
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