참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,1,1-Trifluoro-2-iodoethane | HCID 67709 | — |
| 반응물 | 6-Methylpyridine-3-carbonitrile | HCID 281995 | — |
| 반응물 | Lithium diisopropylamine | HCID 45051747 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6-(3,3,3-Trifluoropropyl)pyridine-3-carbonitrile | HCID 66803134 | 95.4% |
반응 단계
To a solution of 6-methyl-nicotinonitrile (118 mg, 1.0 mmol) in anhydrous THF (20 mL) at −78 C under nitrogen was added lithium diisopropylamine (2M solution in THF/heptane/ethylbenzene, 550 μL, 1.1 mmol) drop-wise. The resulting solution was allowed to warm to room temperature for 5 min and then cooled back to −78 C. 1,1,1-Trifluoro-2-iodo-ethane (524 mg, 2.5 mmol) was then added to the solution drop-wise and the reaction mixture was allowed to warm to room temperature and stirred at this temperature for 2 h. The reaction mixture was cooled at 0 C and quenched with water; the resulting solution was extracted with EtOAc (3×25 mL). Combined organics were washed with brine (25 mL), dried over magnesium sulfate and purified by silica chromatography (25% EtOAc in heptane) to afford the title compound as a pale yellow oil (191 mg, 95%). Method C HPLC-MS: MH+ requires m/z=201. Found: m/z=201, Rt=1.22 min (86%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08895733B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-f6be5aa66dff4bb1bc328e771b783470 |
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| 출처 메모 | uspto-grants-2014_11 |
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