Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N,N'-Dicyclohexylurea | HCID 4277 | — |
Reaction Steps
The above product (0.75 g, 0.0024 mole) is dissolved in 50 ml ethyl acetate. This is cooled to -5° C. and p-nitrophenol is added followed by the portionwise addition of dicyclohexylcarbodiimide. The reaction mixture is stirred at -5° C. for 2 hours. The formed dicyclohexylurea is filtered off. After concentrating to a 10 ml volume, the reaction mixture is cooled overnight. More dicyclohexylurea is formed. This is filtered and the filtrate is concentrated in vacuo to yield 0.95 g of active ester, (the p-nitrophenyl ester of N-[N-[2-(mercaptomethyl)-4-methyl-1-oxopentyl]glycyl]glycine).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04424354 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-687e8519f6564965b2c3d04bd09292b6 |
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| Source note | uspto-grants-1984_01 |
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