関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | 1-Bromo-4-methoxy-2-methylbenzene | HCID 117915 | — |
| 生成物 | 5-Bromo-2-methoxy-4-methylbenzenesulfonic acid dihydrate | HCID 88219692 | 86% |
反応手順
4-Bromo-3-methylanisole (500 g, 2.5 moles) was cautiously added dropwise over a period of 20-25 minutes to 98% sulfuric acid (1,600 ml) at ambient temperature (exothermic, temperature rise to 42-43° C.) and the reaction stirred for 16 hours. The reaction mixture was cautiously quenched onto cooled (0-5° C.) deionised water (7.5 liter) over a 2 hour period at a rate that maintained the temperature below 20° C. The precipitated product was granulated for 3 hours, filtered and dried to give the crude sulphonic acid (980 g). The crude product was recrystallised from ethyl acetate (2.94 liters, 3 ml/g) to give the subtitle compound (680 g, 86% yield) as a white crystalline solid (mp=131-133° C.)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06211223B1 |
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| 出典データセット | uspto-grants-2001_04 |
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| ORD ID | ord-442072f131d44a8b8e579264d4dce522 |
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| 出典メモ | uspto-grants-2001_04 |
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