関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Propargyl bromide | HCID 7842 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2-(2-(2-Hydroxyethoxy)ethyl)-1H-isoindole-1,3(2H)-dione | HCID 2755406 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-[2-(2-Phthalimidoethoxy)ethoxy]propyne | HCID 22226407 | 36.6% |
反応手順
To a stirred solution of compound 15 (1.39 g, 5.91 mmol) in N,N-dimethylformamide (25 mL) was added NaH (0.33 g, 80%) dropwise. After complete NaH addition, stirring was continued for 0.5 h at room temperature and then cooled to 0° C. Propargyl bromide 4 (1.24 mL, 11.13 mmol) was added, and stirring was continued for 0.5 h at 0° C., then for 2 h at room temperature. After careful addition of methanol to decompose excess NaH, the solvent was evaporated and crude product was purified by flash column chromatography (3:2 to 1:1 to 2:3 hexane-ethyl acetate) to give compound 16 as a solid (591 mg, 36.6%) having an RF of 0.41 (solvent 3:2 hexane-ethyl acetate). See FIG. 9.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07019128B2 |
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| 出典データセット | uspto-grants-2006_03 |
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| ORD ID | ord-c37ca55bc09b457898135ea4565144b8 |
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| 出典メモ | uspto-grants-2006_03 |
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