1-Iodopropane → 4-(3-Methoxy-4-nitrophenyl)-1-propylpyridinium iodide

HRID 419473노트

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HRID 419473 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)[CH:6]=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10].[I:18][CH2:19][CH2:20][CH3:21]>CC(=O)C(C)(C)C.CC(C)=O>[I-:18].[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:12]2[CH:17]=[CH:16][N+:15]([CH2:19][CH2:20][CH3:21])=[CH:14][CH:13]=2)[CH:6]=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10]

참가 물질

5

반응물 2

HCID 336431-IodopropaneHCID 137288334-(3-Methoxy-4-nitrophenyl)pyridine

생성물 1

HCID 666496524-(3-Methoxy-4-nitrophenyl)-1-propylpyridinium iodide수율 65.6%

시약·촉매·용매 2

HCID 180Acetone용매HCID 6416Pinacolone용매

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온도
102 °C

실험 절차

To 4-[3-(methyloxy)-4-nitrophenyl]pyridine (5 g, 21.72 mmol) in 50 mL of pinacolone was added, 1-iodopropane (14.77 g, 86.87 mmol). The mixture was heated to 102° C. for 24 h. The mixture was cooled and diluted with acetone. The resulting slurry was filtered and washed with acetone. The product was dried under vacuum to give the title compound of step B (5.7 g, 14.24 mmol, 65%). 1H NMR (400 MHz, DMSO-d6) δ ppm 9.22 (d, J=6.78 Hz, 2H), 8.64 (d, J=6.78 Hz, 2H), 8.09 (d, J=8.42 Hz, 1H), 7.90 (d, J=1.65 Hz, 1H), 7.75 (dd, J=8.42, 1.65 Hz, 1H), 4.59 (t, J=7.33 Hz, 2H), 4.06 (s, 3H), 1.91-2.01 (m, 2H), 0.90 (t, J=7.33 Hz, 3H).

후처리

  1. temperatureThe mixture was cooled
  2. filtrationThe resulting slurry was filtered
  3. washwashed with acetone
  4. customThe product was dried under vacuum

출처 및 근거

ORD 기록
ord-06ea7770fe8a4dfbadd7b5061b94a969
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08093239B2

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