Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | HCID 20378886 | HCID 20378886 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178469093 | HCID 178469093 | — |
Reaction Steps
In 200 ml of ethanol were dissolved 28.6 g of the p-ethoxycarbonylphenyl β-(p-aminophenyl)-propionate hydrochloride obtained and 4.2 g of cyanamide, and the solution was subjected to reaction at 70° C. for 5 hours. After the reaction, the solvent was removed by distillation under reduced pressure to obtain an oily product, to which a mixture consisting of ethanol and diethyl ether was added and the solution was cooled, upon which crystals precipitated. The crystals were collected by filtration and recrystallized from an ethanol-diethyl ether mixture to obtain p-ethoxycarbonylphenyl β-(p-guanidinophenyl)propionate hydrochloride in the form of colorless crystals. Yield: 25.1 g (78%); melting point: 125°-127° C.; IR (cm-1): 3500-2550, 1750, 1708, 1670, 1599; MS: M+= m/e 355 (M.W. - HCl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04182897 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-868098a077504b33ae39c74fbf58b9a9 |
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| Source note | uspto-grants-1980_01 |
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