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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | tert-butyl N-(2-hydroxyethyl)carbamate | HCID 2733206 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl [2-(4-nitrophenoxy)ethyl]carbamate | HCID 18173671 | 72.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06300368B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-88b1ca34415847179a460dafe3905eb7 |
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| Source note | uspto-grants-2001_10 |
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