Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594355Generated: October 26, 2026

Hydrochloric Acid → Ethyl 4-([1,1'-biphenyl]-2-yl)-4-amino-2-methylbutanoate

https://huagongshe.com/reaction/594355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
ReactantEthyl 4-([1,1'-biphenyl]-2-yl)-4-(1,1-dimethylethylsulfinamido)-2-methylbutanoateHCID 86695627—
SolventMethanolHCID 887—
ProductEthyl 4-([1,1'-biphenyl]-2-yl)-4-amino-2-methylbutanoateHCID 69082640—

Reaction Conditions

Temperature0 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-d2e3b08f030840b391ebfbf2f89b644c
Source noteuspto-grants-2016_01