Acetonitrile → 4-(5-(Trifluoromethyl)pyridin-2-yl)benzaldehyde
반응식
[CH:1]([C:3]1[CH:8]=[CH:7][C:6](B(O)O)=[CH:5][CH:4]=1)=[O:2].[F:12][C:13]([F:46])([F:45])[C:14]1[CH:19]=[CH:18][C:17](C2N=CC(NC(C3C=CC(C(NCCC(O)=O)=O)=CC=3)CCC)=CN=2)=C[CH:15]=1.C([O-])([O-])=O.[Na+].[Na+].C(#[N:55])C>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[F:12][C:13]([F:46])([F:45])[C:14]1[CH:19]=[CH:18][C:17]([C:6]2[CH:7]=[CH:8][C:3]([CH:1]=[O:2])=[CH:4][CH:5]=2)=[N:55][CH:15]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 4-formylphenylboronic acid (100 g, 0.67 mol) and 2-chloro-5-(trifluoromethyl)pyridine 2 (121 g, 0.67 mol) in acetonitrile (900 mL) was added Pd(dppf)Cl2 (24 g, 33.5 mmol) and 2M aqueous Na2CO3 (837 mL). The resulting mixture was heated at reflux for 3 h under nitrogen atmosphere. The reaction mixture was extracted with ethyl acetate (3*500 mL). The combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography to give 4-(5-(trifluoromethyl)pyridin-2-yl)benzaldehyde (115 g) as a light yellow solid. 1H NMR (400 MHz CDCl3) δ10.04 (s, 1H), 8.92 (s, 1H), 8.15 (d, J=8.0 Hz, 2H), 7.98 (d, J=8.0 Hz, 1H), 7.96 (d, J=8.0 Hz, 2H), 7.86 (d, J=8.0 Hz, 1H). MS (M+1)=252.0.
후처리
- temperatureThe resulting mixture was heated
- temperatureat reflux for 3 h under nitrogen atmosphere
- extractionThe reaction mixture was extracted with ethyl acetate (3*500 mL)
- dry with materialThe combined organic layers were dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe crude material was purified by silica gel chromatography
출처 및 근거
- ORD 기록
- ord-fe263ae3d6f54f9d8feac645b7fb5d8d
- 출처 데이터셋
- uspto-grants-2015_01
- 특허 번호
- US08933104B2
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