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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21526Generated: October 30, 2026

Ethyl Acetate → Methyl {o-{5-[2-chloro-4-(methylsulfinyl)phenoxy]-2-nitrophenoxy}phenoxy}acetate

https://huagongshe.com/reaction/21526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 53873458HCID 53873458—
SolventDichloromethaneHCID 6344—
ProductMethyl {o-{5-[2-chloro-4-(methylsulfinyl)phenoxy]-2-nitrophenoxy}phenoxy}acetateHCID 5425775558.7%

Reaction Steps

A solution of methyl {o-{5-[2-chloro-4-(methylthio)phenoxy]-2-nitrophenoxy}phenoxy}acetate (4.30 g, 0.009 mol) in methylene chloride is cooled to 0° C. and treated with 3-chloroperoxybenzoic acid (1.73 g, 0.010 mol). The reaction mixture is warmed to room temperature, stirred overnight, quenched with triethylamine (1.4 mL) and concentrated in vacuo. The residue is dissolved into ethyl acetate and the organic solution is washed sequentially with water and 2 N hydrochloric acid, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain an amber oil. Column chromatography of the oil using silica gel and ethyl acetate gives the title product as an amber oil (2.6 g) which is identified by NMR spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424280
Source datasetuspto-grants-1995_06
ORD IDord-a8b9a9641653481db5a68fae31d5cdd0
Source noteuspto-grants-1995_06