참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,8-Dibromooctane | HCID 78310 | — |
| 반응물 | Lithium Chloride | HCID 433294 | — |
| 반응물 | HCID 178418370 | HCID 178418370 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 8-(4-Methylphenyl)octylbromide | HCID 19930262 | — |
반응 단계
Lithium chloride (0.15 g, 3.5 mmol) and cupric chloride (0.3 g, 2.2 mmol) were added to THF (100 ml) and stirred for 1 hour 30 minutes. 1,8-Dibromooctane (37 g, 137 mmol) was then added. While keeping the temperature between 0° C. and 5° C., 4-methylphenyl magnesium bromide in THF (prepared from magnesium (2.3 g, 95 mmol) and 4-methylphenyl bromide (15.4 g, 90 mmol) in THF (150 ml)) was added over 1 hour, allowing the temperature to reach room temperature overnight. The reaction mixture was poured over concentrated hydrochloric acid/ice mixture and the product was extracted into ether. The ether was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulphate and evaporated to give an oil, which was distilled under vacuum to give 8-(4-methylphenyl)octylbromide as an oil, bp 128° at 0.2mm.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05428065 |
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| 출처 데이터셋 | uspto-grants-1995_06 |
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| ORD ID | ord-3c0ab915b7924fe2ab78fabd3f338f32 |
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| 출처 메모 | uspto-grants-1995_06 |
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