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Phosphorus oxychloride → 2,4-Dichloro-7-(1-ethylpropyl)-1-methyl-1H-benzimidazole

HRID 1698557
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인쇄 미리보기

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HRID 1698557 반응식
[Cl:1][C:2]1[C:10]2[NH:9][C:8](=O)[N:7]([CH3:12])[C:6]=2[C:5]([CH:13]([CH2:16][CH3:17])[CH2:14][CH3:15])=[CH:4][CH:3]=1.P(Cl)(Cl)([Cl:20])=O>>[Cl:20][C:8]1[N:7]([CH3:12])[C:6]2[C:5]([CH:13]([CH2:16][CH3:17])[CH2:14][CH3:15])=[CH:4][CH:3]=[C:2]([Cl:1])[C:10]=2[N:9]=1
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참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 672724674-Chloro-7-(1-ethylpropyl)-1-methyl-1,3-dihydro-2H-benzimidazol-2-one

생성물 1

HCID 672730252,4-Dichloro-7-(1-ethylpropyl)-1-methyl-1H-benzimidazole수율 82%

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온도
90 °C

실험 절차

A mixture of 4-chloro-7-(1-ethylpropyl)-1-methyl-1,3-dihydro-2H-benzimidazol-2-one (1.17 g, 4.63 mmol) in phosphorous oxychloride (28 g) was stirred at 90° C. for 3 h. The reaction was allowed to cool to room temperature and concentrated in vacuo. The residue was dissolved in ethyl acetate, washed with aqueous sodium bicarbonate and brine. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was subjected to chromatography on silica gel (n-hexane/ethyl acetate=10:1-1:1) and crystallized from ethyl acetate-hexane to afford the title compound as colorless crystals (1.03 g, 82%). mp 94-95° C.

후처리

  1. temperatureto cool to room temperature
  2. concentrationconcentrated in vacuo
  3. dissolutionThe residue was dissolved in ethyl acetate
  4. washwashed with aqueous sodium bicarbonate and brine
  5. dry with materialThe organic layer was dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customcrystallized from ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-5bcab18d8a724af8b5894e1be5986677
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08163935B2

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