참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | 1-Bromo-4-methoxy-2-methylbenzene | HCID 117915 | — |
| 생성물 | 5-Bromo-2-methoxy-4-methylbenzenesulfonic acid dihydrate | HCID 88219692 | 86% |
반응 단계
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.)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06211223B1 |
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| 출처 데이터셋 | uspto-grants-2001_04 |
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| ORD ID | ord-442072f131d44a8b8e579264d4dce522 |
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| 출처 메모 | uspto-grants-2001_04 |
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