참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isoquinoline | HCID 8405 | — |
| 반응물 | Sodium aluminate | HCID 14766 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 반응물 | Aluminum | HCID 5359268 | — |
| 반응물 | Aluminum(III) Chloride | HCID 6451240 | — |
| 생성물 | 5-Bromoisoquinoline | HCID 736487 | 26% |
반응 단계
The apparatus was a 500 mL three-necked flask equipped with a condenser, dropping funnel, and a stirrer terminating in a stiff, crescent-shaped Teflon polytetrafluroethylene paddle. To the isoquinoline (57.6 g, 447 mmol) in the flask was added AlCl3 (123 g, 920 mmol). The mixture was heated to 75–85° C. Bromine (48.0 g, 300 mmol) was added using a dropping funnel over a period of 4 hours. The resulting mixture was stirred for one hour at 75° C. The almost black mixture was poured into vigorously hand-stirred cracked ice. The cold mixture was treated with sodium hydroxide solution (10 N) to dissolve all the aluminum salts as sodium aluminate and the oily layer was extracted with ether. After being dried with Na2SO4 and concentrated, the ether extract was distilled at about 0.3 mm. A white solid (16.3 g, 78 mmol) from a fraction of about 125° C. was obtained (26% yield). The product was further purified by recrystallization (pentane or hexanes): mp 80–81° C.;
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091212B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-b9469d6f4a4846c6b2874fbf0254c2dd |
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| 출처 메모 | uspto-grants-2006_08 |
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