참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1,1-Bis(hydroxymethyl)cyclopropane | HCID 4101437 | — |
| 반응물 | 1-Fluoro-4-iodo-2-nitrobenzene | HCID 14590582 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (1-((4-Iodo-2-nitrophenoxy)methyl)cyclopropyl)methanol | HCID 86693527 | 71% |
반응 단계
A solution of 1-fluoro-4-iodo-2-nitrobenzene (2.50 g, 9.4 mmol) in DMF (30 mL) was treated with 1-(hydroxymethyl)cyclopropylmethanol (1.91 g, 19 mmol) and K2CO3 (2.6 g, 19 mmol) and the mixture was heated at 50° C. for 8 hours. TLC indicated complete consumption of the arylfluoride. The mixture was diluted with water and extracted with ethyl acetate. The combined organics were washed with brine, dried over sodium sulfate and concentrated by rotoevaporation. Purification by flash column chromatography (EtOAc in heptanes) gave the titled compound as a light yellow solid (2.31 g, 71% yield). 1H NMR (400 MHz, DMSO) δ 8.15 (d, J=2.2 Hz, 1H), 7.92 (dd, J=8.8, 2.2 Hz, 1H), 7.17 (d, J=8.9 Hz, 1H), 4.60 (t, J=5.6 Hz, 1H), 4.05 (s, 2H), 3.36 (d, J=5.6 Hz, 2H), 0.50 (s, 4H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09034866B2 |
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| 출처 데이터셋 | uspto-grants-2015_05 |
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| ORD ID | ord-af1aafb3e9064f4bac3bdba56441a578 |
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| 출처 메모 | uspto-grants-2015_05 |
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