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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308899Generated: October 26, 2026

Ethyl Acetate → 2-[(2-Chloro-6-nitrophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone

https://huagongshe.com/reaction/2308899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Bromomethyl)-1-chloro-3-nitrobenzeneHCID 91858—
Reactant4,4-Dimethyl-1,2-oxazolidin-3-oneHCID 642151—
Catalyst18-Crown-6HCID 28557—
SolventAcetonitrileHCID 6342—
Product2-[(2-Chloro-6-nitrophenyl)methyl]-4,4-dimethyl-3-isoxazolidinoneHCID 1393494452.7%

Reaction Steps

A mixture of 2-chloro-6-nitrobenzyl bromide (17.5 g, 0.07 mole), 4,4-dimethyl-3-isoxazolidinone (11.5 g, 0.1 mole), potassium carbonate (13.8 g, 0.1 mole), and 1,4,7,10,13,16-hexaoxacyclooctadecane (0.5 g, 0.002 mole) in acetonitrile (500 ml) was stirred at ambient temperature overnight. The reaction mixture was poured into ethyl acetate (500 ml) and the mixture washed with water (3×200 ml). The dried (magnesium sulfate) ethyl acetate layer was concentrated under reduced pressure to yield a liquid. The liquid product was subjected to chromatography on silica gel, eluting with 1:9 ethyl acetate:heptane. The appropriate fractions were combined and concentrated under reduced pressure to yield a white solid. The solid was recrystallized from ethyl acetate to yield 10.5 g of 2-[(2-chloro-6-nitrophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone, m.p. 86°-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04692182
Source datasetuspto-grants-1987_09
ORD IDord-72a1f803fa9f4c17acf7237769c045bd
Source noteuspto-grants-1987_09