참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Fluoroethanol | HCID 9737 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 3-Bromobenzyl bromide | HCID 69979 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Bromo-3-(2-fluoroethoxymethyl)benzene | HCID 15058770 | 58% |
반응 단계
A mixture of sodium hydride [60% in oil] (343, mg, 8.6 mmol) and THF at −5° C. was treated via a syringe with a solution of 2-fluoroethanol in THF over a 1 min. period, stirred for 2 min., warmed to room temperature, stirred for 15 min. at room temperature, treated with 3-bromobenzylbromide (2.5 g, 11.7 mmol), stirred for 1 h, poured into saturated ammonium chloride and extracted with ether. The extracts were combined, washed sequentially with water and brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel, 20:1 hexane/ ethyl acetate as eluent, to afford 1-bromo-3-(2-fluoroethoxymethyl)benzene as a yellow oil, 1 g (58% yield), 1H NMR (DMSO-d6) δ 3.6 (dxt, 2H); 4.5 (dxt, 2H); 4.4 (s, 2 H); 7.3 (m, 2H); 7.5 (m, 2H); MS [(+)ESI] m/z 219 [M−H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07423158B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-158d176688544e6aa2e5b276473b5061 |
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| 출처 메모 | uspto-grants-2008_09 |
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