HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Ethyl 4-([1,1'-biphenyl]-2-yl)-4-amino-2-methylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Ethyl 4-([1,1'-biphenyl]-2-yl)-4-(1,1-dimethylethylsulfinamido)-2-methylbutanoate | HCID 86695627 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl 4-([1,1'-biphenyl]-2-yl)-4-amino-2-methylbutanoate | HCID 69082640 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A cooled (0° C.) slightly yellow solution of ethyl 4-([1,1′-biphenyl]-2-yl)-4-(1,1-dimethylethylsulfinamido)-2-methylbutanoate (220 mg; 0.54 mmol) in MeOH (3 ml) was treated dropwise with a solution of 4 M HCl in 1,4-dioxane (0.27 ml; 1.08 mmol). The resulting yellow mixture was further stirred at 0° C., under nitrogen, for 10 min., and then at rt for 1 h. The reaction mixture was then concentrated to dryness under reduced pressure and the oily residue was further dried under HV to give the chlorhydrate salt of ethyl 4-([1,1′-biphenyl]-2-yl)-4-amino-2-methylbutanoate. LC-MS (conditions A): tR=0.63 min.; [M+H]+: 298.22 g/mol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242970B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-d2e3b08f030840b391ebfbf2f89b644c |
| Source note | uspto-grants-2016_01 |