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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227756Generated: October 30, 2026

Ethyl bromoacetate → Ethyl(4-[2-methyl-2-nitropropyl]phenoxy)ethanoate

https://huagongshe.com/reaction/2227756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Methyl-2-nitropropyl)phenolHCID 12826902—
ProductEthyl(4-[2-methyl-2-nitropropyl]phenoxy)ethanoateHCID 2214773797.4%

Reaction Steps

A mixture of 4-(2-methyl-2-nitropropyl)phenol (3.0 g, 15.4 mmol), ethylbromoacetate (2.04 mL, 17.0 mmol) and potassium carbonate (6.4 g, 46.2 mmol) was stirred at room temperature for 18 h. The reaction was concentrated in vacuo and the resulting residue partitioned between EtOAc and water. The layers were separated and the aqueous layer extracted with EtOAc (3×). The combined organic layers were washed with water (3×), brine, dried (Na2SO4), and concentrated in vacuo to a brown oil. The material was purified by flash chromatography over silica gel eluting with 5% MeOH/CHCl3 to provide 4.22 g (97%) of a clear oil. NMR

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413991B1
Source datasetuspto-grants-2002_07
ORD IDord-02088a05a7924011bf518c7743a3c429
Source noteuspto-grants-2002_07