関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | (4-Methoxymethoxy-phenylethynyl)-trimethylsilane | HCID 10657368 | — |
| 反応物 | HCID 178446069 | HCID 178446069 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 5-(2-Trimethylsilylethynyl)-2-methoxymethoxybenzaldehyde | HCID 19701592 | — |
反応手順
A solution of 4-(2-trimethylsilylethynyl)phenol methoxymethyl ether (6.08 g) in diethyl ether (450 ml) was cooled to -78° C., to which was added dropwise, under argon atmosphere, a 1.7M t-butyl lithium pentane solution (18 ml), and the mixture was stirred for one hour at the same temperature. To the reaction mixture was then added dropwise DMF(5 ml), followed by warming up to room temperature and stirring overnight. To the reaction mixture were added ethyl acetate and water, which was subjected to extraction. The organic layer was washed (a saturated aqueous saline solution) and dried (anhydrous magnesium sulfate), followed by distilling off the solvent under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluted with ethyl acetate/hexane) to give 5-(2-trimethylsilylethynyl)-2-methoxymethoxybenzaldehyde (5.29 g) (Compound B-27). The physical properties are shown in Table 8.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05716971 |
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| 出典データセット | uspto-grants-1998_02 |
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| ORD ID | ord-01eb2cf2a43c4d479d27f41b864bad98 |
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| 出典メモ | uspto-grants-1998_02 |
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