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[Br:1][C:2]1[CH:3]=[N:4][C:5](C#N)=[N:6][CH:7]=1.C[Mg]Br.[CH2:13]1[CH2:17][O:16]CC1>>[Br:1][C:2]1[CH:3]=[N:4][C:5]([C:17](=[O:16])[CH3:13])=[N:6][CH:7]=1참가 물질
4
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- 온도
- -78 °C
실험 절차
To a solution of 5-bromopyrimidine-2-carbonitrile (221 mg, 1.2 mmol) in THF (10 ml) was added methylmagnesium bromide (3.0 ml, 4.20 mmol, 1.4 molar, THF) at −78° C. under nitrogen. The solution was stirred at −78° C. for 3.5 hours, and then quenched with satd aq NH4Cl, and extracted with EtOAc. The combined organic layer was dried over anhydrous Na2SO4 and concentrated. The reaction was purified by column chromatography on silica gel (petroleum ether: EtOAc=1:0 to 0:1) to afford 1-(5-bromopyrimidin-2-yl)ethanone (1.55 mg, 61% yield). 1H NMR (CDCl3 500 MHz): δ 9.00 (s, 2H), 2.80 (s, 3H).
후처리
- customquenched with satd aq NH4Cl
- extractionextracted with EtOAc
- dry with materialThe combined organic layer was dried over anhydrous Na2SO4
- concentrationconcentrated
- customThe reaction was purified by column chromatography on silica gel (petroleum ether: EtOAc=1:0 to 0:1)
출처 및 근거
- ORD 기록
- ord-71a37e665ded4f3a9f8e1cbfe2daea43
- 출처 데이터셋
- uspto-grants-2015_08
- 특허 번호
- US09108938B2
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