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Methyl iodide → 4-[4-(Dimethylamino)phenyl]-1-methylpyridin-1-ium iodide

HRID 240219
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인쇄 미리보기

반응식

HRID 240219 반응식
[CH3:1][N:2]([CH3:15])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][N:12]=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.[CH3:16][I:17]>C(#N)C>[I-:17].[CH3:1][N:2]([CH3:15])[C:3]1[CH:4]=[CH:5][C:6]([C:9]2[CH:10]=[CH:11][N+:12]([CH3:16])=[CH:13][CH:14]=2)=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6328Methyl iodideHCID 227783N,N-dimethyl-4-(pyridin-4-yl)aniline

생성물 1

HCID 132272704-[4-(Dimethylamino)phenyl]-1-methylpyridin-1-ium iodide

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

N,N-dimethyl-4-(pyridine-4-yl)aniline (0.15 g, 7.6 mmols) was dissolved in acetonitrile (50 ml) and methyl iodide (4 ml) was added. The mixture was heated at reflux for 4 hrs then cooled to ambient temperature. IDT307 (0.17 g, 5 mmols) crystallized upon standing and was removed via filtration. 1H NMR (DMSO-d6) δ 3.40 (s, 6H), 4.25 (s, 3H), 6.92 (d, 2H), 8.06 (d, 2H), 8.38 (d, 2H), 8.80 (d, 2H).

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 4 hrs
  3. customIDT307 (0.17 g, 5 mmols) crystallized
  4. customwas removed via filtration

출처 및 근거

ORD 기록
ord-a35eba22304a40beb12a5a0dfb6f00a9
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08647827B2

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