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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379693Generated: October 30, 2026

4-Nitrophenol → tert-Butyl [2-(4-nitrophenoxy)ethyl]carbamate

https://huagongshe.com/reaction/379693

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl [2-(4-nitrophenoxy)ethyl]carbamateHCID 1817367172.6%

Reaction Steps

4-Nitrophenol (4.01 g), 2-(tert-butoxycarbonylamino)ethanol (4.65 g) and triphenylphosphine (7.55 g) were dissolved into tetrahydrofuran (50 ml) and the solution was ice cooled. Azo dicarboxylic acid diethyl (5.52 g) dissolved in tetrahydrofuran (5 ml) was added drop-wise into the ice-cooled solution. After being stirred for one hour at room temperature, the reaction mixture was concentrated under vacuum. Residue was dissolved into ethyl acetate (50 ml). Hexane (400 ml) was added to the ethyl acetate solution and insoluble matter formed was removed from solution by filtration. Filtrate was concentrated under vacuum to small volume. Concentrate was purified by silica-gel column chromatography using ethyl acetate:hexane (1:1) as the solvent system to obtain N-(tert-butoxycarbonyl)-2-(4-nitrophenoxy)ethylamine (5.91 g) as color-less oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300368B1
Source datasetuspto-grants-2001_10
ORD IDord-88b1ca34415847179a460dafe3905eb7
Source noteuspto-grants-2001_10