HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Chloromethyl Methyl Ether → 3-Methoxymethyloxyphthalic anhydride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Chloromethyl Methyl Ether | HCID 7864 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 3-Hydroxyphthalic anhydride | HCID 96580 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-Methoxymethyloxyphthalic anhydride | HCID 21936735 | 95,1% |
Reaktionsschritte
To a solution of 4-hydroxy-isobenzofuran-1,3-dione (0.5 g, 3.03 mmol) in anhydrous N,N-dimethylformamide (6 ml) under nitrogen was added diisopropylethylamine (1.05 ml, 6.06 mmol). The solution was stirred with cooling in an ice bath and chloromethyl methyl ether (0.46 ml, 6.06 mmol) was added. The reaction was allowed to slowly warm to ambient temperature and then stirred for an additional 7 h. The mixture was concentrated in vacuo to a small volume and diluted with ethyl acetate (75 ml). The organic layer was washed with water (2×40 ml), brine (20 ml), dried (Na2SO4), filtered, and the solvent evaporated in vacuo to give 0.6 g (95%) of 4-methoxymethoxy-isobenzofuran-1,3-dione as a solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07115624B1 |
| Quelldatensatz | uspto-grants-2006_10 |
| ORD ID | ord-9c159aa09fca4c05ba10f78ada78664b |
| Quellennotiz | uspto-grants-2006_10 |