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Chloromethyl Methyl Ether → 3-Methoxymethyloxyphthalic anhydride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chloromethyl Methyl Ether | HCID 7864 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 3-Hydroxyphthalic anhydride | HCID 96580 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-Methoxymethyloxyphthalic anhydride | HCID 21936735 | 95.1% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07115624B1 |
| 出典データセット | uspto-grants-2006_10 |
| ORD ID | ord-9c159aa09fca4c05ba10f78ada78664b |
| 出典メモ | uspto-grants-2006_10 |