Dimethylformamide → ethyl 8-iodo-7-methoxy-2-(trifluoromethyl)-2H-chromene-3-carboxylate
반응식
[OH:1][C:2]1[C:9]([I:10])=[C:8]([O:11][CH3:12])[CH:7]=[CH:6][C:3]=1[CH:4]=O.[F:13][C:14](/[C:17](=C\C)/C(OCC)=O)([F:16])[F:15].C(=O)([O-])[O-].[Cs+].[Cs+].CN(C)C=O.[C:36]([O:39][CH2:40][CH3:41])(=[O:38])[CH3:37]>>[I:10][C:9]1[C:8]([O:11][CH3:12])=[CH:7][CH:6]=[C:3]2[C:2]=1[O:1][CH:17]([C:14]([F:16])([F:15])[F:13])[C:37]([C:36]([O:39][CH2:40][CH3:41])=[O:38])=[CH:4]2참가 물질
반응 조건
- 온도
- 90 °C
실험 절차
To the mixture of 1.5 g (5.4 mmol) of 2-hydroxy-3-iodo-4-methoxybenzaldehyde, 3.1 mL (20.6 mmol) of ethyl trifluoromethylcrotonate, and 4.2 g(12.9 mmol) of cesium carbonate was added 8 mL of anhydrous N,N-dimethylformamide. The mixture was heated to 90° C. overnight. After cooling to room temperature, to the reaction was added 150 mL of ethyl acetate. The organic solution was filtered, washed with brine and dried over anhydrous magnesium sulfate. After removing the volatiles, the residue was purified by silica chromatography with ethyl acetate/hexane (2:8) to give 0.3 g (14%) a light yellow solid: 1H NMR(CDCl3/400 MHz) 7.65(s, 1H), 7.17(d, J=8.4 Hz, 1H), 6.50(d, J=8.4 Hz, 1H), 5.80(q, J=6.8 Hz,1H), 4.30(m, 2H), 3.92(s, 3H), 1.33(t, J=7.6 Hz, 3H). MS (ESI+) 429.0(M+1, 100). HRMS (EI+) m/z calcd for (C14H12F3O4) 427.9732, found 427.9715.
후처리
- temperatureAfter cooling to room temperature, to the reaction
- filtrationThe organic solution was filtered
- washwashed with brine
- dry with materialdried over anhydrous magnesium sulfate
- customAfter removing the volatiles
- customthe residue was purified by silica chromatography with ethyl acetate/hexane (2:8)
출처 및 근거
- ORD 기록
- ord-85b4db35c8b64128bac6b94fbe2ef3c4
- 출처 데이터셋
- uspto-grants-2007_08
- 특허 번호
- US07259266B2
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