HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 4-nitro-3-phenyl-L-alaninate monohydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Nitro-3-phenyl-L-alanine | HCID 13706 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | Ethyl 4-nitro-3-phenyl-L-alaninate monohydrochloride | HCID 6453710 | — |
Reaction Steps
4-nitrophenylalanine (5 g, 1 eq, mmol) was added in portions to a solution of dry ethanol (50 mL) and thionylchloride (5 mL) at −5° C. It was stirred at that temperature for another one hour, followed by stirring at RT for 16 h. The reaction mixture was condensed on rotavapour, azeotroped with toluene, and then dried over high vaccum pump to obtain 4-nitrophenylalanine ethyl ester hydrochloride as white solid (quantitative yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07314889B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-d899ea73723646ffa3614f7d692e309a |
| Source note | uspto-grants-2008_01 |