関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Ethyl-6-methylphenol | HCID 519333 | — |
| 反応物 | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 4-Bromo-2-ethyl-6-methylphenol | HCID 22006838 | 182.7% |
反応手順
Then, 16 g of 2-ethyl-6-methylphenol was dissolved in 200 ml of chloroform, which was stirred at 0° C., and 56.6 g of tetrabutylammonium tribromide was added in small portions to this solution. After stirring at room temperature for 1 hour, the solvent was distilled out under reduced pressure. The residue was dissolved in 300 ml of diethyl ether, successively washed with 10% hydrochloric acid and water, dried over anhydrous magnesium sulfate, and then concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 23 g of 4-bromo-2- ethyl-6-methylphenol (92% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06214835B1 |
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| 出典データセット | uspto-grants-2001_04 |
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| ORD ID | ord-f0caecc358eb4b89a5c7f398cc8089aa |
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| 出典メモ | uspto-grants-2001_04 |
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