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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325033Generated: October 26, 2026

t-Butoxycarbonylamino-3-[2-(4-cyanophenyl)ethoxy]-2-methylbenzene → Amino-3-[2-(4-cyanophenyl)ethoxy]-2-methylbenzene

https://huagongshe.com/reaction/325033

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-Butoxycarbonylamino-3-[2-(4-cyanophenyl)ethoxy]-2-methylbenzeneHCID 22033517—
SolventHydrochloric AcidHCID 313—
SolventEthyl AcetateHCID 8857—
ProductAmino-3-[2-(4-cyanophenyl)ethoxy]-2-methylbenzeneHCID 2203354021.8%

Reaction Steps

t-Butoxycarbonylamino-3-[2-(4cyanophenyl)ethoxy]-2-methylbenzene (2.69 g, 7.64 mmol; from step (ii) above) were dissolved in EtOAc, pre-saturated with HCl(g), (150 mL) under nitrogen and stirred at room temperature overnight. After evaporation of the solvent the residue was partitioned between 10% aqueous HCl and EtOAc. The aqueous phase was washed with EtOAc, basified with NaOH (2M, aq.) and extracted with EtOAc. The combined organic phases were washed with brine, dried (MgSO4) and the solvent evaporated to afford 0.42 g (19%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06221898B1
Source datasetuspto-grants-2001_04
ORD IDord-2c5a44f5757b46c7a556afb552752caf
Source noteuspto-grants-2001_04