関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Bromomethylstyrene | HCID 98116 | — |
| 反応物 | 2-Bromo-6-iodo-4-methylphenol | HCID 59344907 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-Bromo-3-iodo-5-methyl-2-(3-phenylallyloxy)-benzene | HCID 68585603 | 101.2% |
反応手順
2-Bromo-4-methyl-6-iodophenol (7.82 gm, 25 mmol) and cinnamyl bromide (4.93 g, 25 mmol) were added to DMF (20 ml). Diisopropylethylamine (5.3 ml, 30.4 mmol) was added and the mixture heated to 60° C. for 15 minutes and then allowed stir for 16 hours at room temperature. The DMF was removed under vacuum, and 1M HCl was added until the residue was acidic. The mixture was extracted with ethyl acetate, and the combined organic phase was dried over magnesium sulfate, filtered, and concentrated under reduced pressure to give 1-bromo-3-iodo-5-methyl-2-(3-phenylallyloxy)-benzene (10.86 g, 100% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07741326B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-c9bb23be4d014b61b2df65620189bc16 |
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| 出典メモ | uspto-grants-2010_06 |
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