참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosphorus oxybromide | HCID 24613 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (3-(5-Methyloxazol-2-yl)phenyl)methanol | HCID 67252704 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(3-(Bromomethyl)phenyl)-5-methyloxazole | HCID 67251165 | 84.5% |
반응 단계
To a stirred solution of (3-(5-methyloxazol-2-yl)phenyl)methanol (0.79 g, 4.13 mmol) in THF (15 mL), POBr3 (1.93 g, 6.61 mmol) was added in portions at 5° C. The reaction mixture was allowed to warm to rt and then heated at 60° C. for 4 h. The mixture was cooled to rt, poured into saturated aqueous NaHCO3 solution and extracted with TBME (2×). The combined organic layers were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash-column chromatography over silicagel (eluent: gradient 5%-40% ethyl acetate/heptane) to yield the title compound (0.88 g, 84%). [1H NMR (400 MHz, CHLOROFORM-d) ♀ ppm 8.01-8.07 (m, 1H), 7.93 (ddd, J=6.7, 2.1, 1.9 Hz, 1H), 7.39-7.47 (m, 2H), 6.85 (d, J=1.3 Hz, 1H), 4.53 (s, 2H), 2.41 (d, J=1.3 Hz, 3H); LCMS RtA=1.10, [M+H]+=252.1/254.1].
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08530648B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-cf9487623ced493abc93547ac99c8ce5 |
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| 출처 메모 | uspto-grants-2013_09 |
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