Reacción #169591
ord-b87c12c2a25949d4a7e27e1e34daf3b9
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otroto afford a precipitate
- 2FiltraciónThe slurry was filtered under nitrogen
- 3Otroto afford a white solid, which
- 4Lavadowas washed with ether
- 5OtroThe solid was dried under vacuum
Procedimiento
A solution of methyl 3-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)propanoate (4 mg, 1.44 mmol) in dioxane (6.0 mL) was treated with 4M HCl in dioxane (about 6.0 mL, 23.0 mmol) at room temperature. The mixture was stirred for 18 hours to completion, after which the reaction mixture was diluted with ether to afford a precipitate. The slurry was filtered under nitrogen to afford a white solid, which was washed with ether. The solid was dried under vacuum to afford the methyl 3-amino-2-(4-chlorophenyl)propanoate hydrochloride as a white solid (321 mg, 89%). LCMS (APCI+) m/z 214.0 [M+H]+.