HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249069Generated: October 26, 2026
4-Nitrophenol → N-Carbobenzoxy-beta-Benzyl-L-Aspartyl-L-Proline p-Nitrophenyl Ester
https://huagongshe.com/reaction/249069
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 54163294 | HCID 54163294 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-Carbobenzoxy-beta-Benzyl-L-Aspartyl-L-Proline p-Nitrophenyl Ester | HCID 53695211 | — |
Reaction Steps
p-Nitrophenol (3.0 Kg) is added to the concentrated ethyl acetate solution of N-carbobenzoxy-β-benzyl-L-aspartyl-L-proline prepared as described in Example II above. The solution is cooled below 5° C. Dicyclohexylcarbodiimide (4.5 Kg) is dissolved in ethyl acetate (10-20 L) and added, maintaining the temperature below 5° C. The solution is stirred at reduced temperature for two hours and then for three hours at 20°-30° C. The dicyclohexylurea is removed by filtration and washed with ethyl acetate (20-30 L). The filtrate is concentrated in vacuo below 60° C. The concentrate is dissolved in hot isopropyl alcohol (50-70 L) and cooled below 25° C. The solids are collected on a filter, rinsed with isopropyl alcohol and dried below 40° C. Melting point=88°-91° C.; specific rotation=-70° to -73° (C=1, ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05212287 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-7363ea10945247a4944f8080ab782600 |
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| Source note | uspto-grants-1993_05 |
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