Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778241Generated: November 2, 2026

Tert-butyl 2-(4-nitrophenoxy)acetate → Tert-butyl 2-(4-aminophenoxy)acetate

https://huagongshe.com/reaction/1778241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-(4-nitrophenoxy)acetateHCID 22061043—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl 2-(4-aminophenoxy)acetateHCID 22060435—

Reaction Steps

Into a 100-mL round-bottom flask, was placed tert-butyl 2-(4-nitrophenoxy)acetate (2 g, 7.74 mmol, 1.00 equip, 98%), Palladium on carbon (200 mg), and methanol (50 mL). To the above hydrogen was introduced. The resulting solution was stirred for 18 h at room temperature. The solids were filtered out. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:10) to yield tert-butyl 2-(4-aminophenoxy)acetate as a reddish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266835B2
Source datasetuspto-grants-2016_02
ORD IDord-4116e8a6e3544f46b9830db3340d5b66
Source noteuspto-grants-2016_02