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Methyl iodide → Diphenoxymethane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl iodide | HCID 6328 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 4-Phenoxyphenol | HCID 13254 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 生成物 | Diphenoxymethane | HCID 78183 | — |
反応手順
4-(Phenoxy)phenol (9.31 g, 50 mmol) in THF (100 mL) was treated with potassium t-butoxide (6.17 g, 55 mmol) at room temperature for 10 min. Methyl iodide (7.87 g, 55 mmol) was added by syringe. After stirring for 18 h at room temperature the reaction was quenched with saturated ammonium chloride solution and diluted with ethyl ether. The separated organic layer was washed with saturated ammonium chloride solution, dried with magnesium sulfate, filtered and concentrated to give 9.98 g of the title compound as a pale yellow oil. GS-MS (m/z, EI): 200 [M]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07119201B2 |
| 出典データセット | uspto-grants-2006_10 |
| ORD ID | ord-191aa6473abc48819fccfa42a9fa38cc |
| 出典メモ | uspto-grants-2006_10 |