참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | Acetyl chloride | HCID 6367 | — |
| 반응물 | 2-Chloroquinoline | HCID 11928 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-Iodoquinoline | HCID 81044 | 70% |
반응 단계
2-Iodoquinoline was prepared according to the procedure of Kimber, et. al. (Tetrahedron 2000, 56, 3575). To a solution of 2-chloroquinoline (10.0 g, 61.5 mmol) in CH3CN (100 mL) was added sodium iodide (14 g, 92.3 mmol) and acetyl chloride (8.8 mL, 123 mmol). The reaction mixture was stirred at 100° C. for 5 hours, then cooled to room temperature and quenched with 10% aqueous K2CO3 (100 mL) and 5% aqueous NaHSO3 (50 mL). The aqueous layer was extracted twice with dichloromethane then the combined organic extracts were dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (0% to 20% EtOAc in hexanes) to provide 9.7 g (70%) of 2-iodoquinoline as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08084623B2 |
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| 출처 데이터셋 | uspto-grants-2011_12 |
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| ORD ID | ord-0e2ad7a8c24944d5ba4f9e2f0eb10044 |
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| 출처 메모 | uspto-grants-2011_12 |
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