HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → Methyl {o-{5-[2-chloro-4-(methylsulfinyl)phenoxy]-2-nitrophenoxy}phenoxy}acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 53873458 | HCID 53873458 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl {o-{5-[2-chloro-4-(methylsulfinyl)phenoxy]-2-nitrophenoxy}phenoxy}acetate | HCID 54257755 | 58.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424280 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-a8b9a9641653481db5a68fae31d5cdd0 |
| Source note | uspto-grants-1995_06 |