Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | HCID 20378929 | HCID 20378929 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178426886 | HCID 178426886 | — |
Reaction Steps
In 200 ml of ethanol were dissolved 21.8 g of the p-methylphenyl α-methyl-β-(p-aminophenyl)-propionate hydrochloride obtained and 4.2 of cyanamide, and the resulting 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. A mixture of ethanol and diethyl ether was added thereto 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-methylphenyl α-methyl-β-(p-guanidinophenyl)propionate hydrochloride in the form of colorless crystals. Yield: 17.4 g (70%); melting point: 146°-148° C.; IR (cm-1): 3500-2550, 1748, 1653, 1631; MS: M+ =m/e 312 (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-d30e731c12874ba293abb3207e2af74c |
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| Source note | uspto-grants-1980_01 |
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