HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → methyl (2S)-2-amino-3-(4-phenylphenyl)propanoate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (S)-Methyl 3-([1,1'-biphenyl]-4-yl)-2-((tert-butoxycarbonyl)amino)propanoate | HCID 10286882 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | methyl (2S)-2-amino-3-(4-phenylphenyl)propanoate hydrochloride | HCID 45357110 | — |
Reaction Steps
To a solution of methyl (S)-2-(t-butoxycarbonylamino)-3-(4-biphenylyl)-propionate (1.25 mmol) in ethyl acetate (2 mL), is added a saturated solution of anhydrous hydrogen chloride in ethyl acetate (4.5 mL). The solution is stirred at room temperature for 3 hours. The reaction mixture is concentrated to obtain methyl (S)-2-amino-3-(4-biphenylyl)-propionate hydrochloride, m.p. 205°-207°; [60 ]D20 +11.8° (c=1, CH3OH), also named (S)-(4-biphenyl)-alanine methyl ester hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155100 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-3ac132f0900446a5a608d87cd49c088d |
| Source note | uspto-grants-1992_10 |