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Phosphorus pentachloride → HCID 67125855, 화합물

HRID 243273
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HRID 243273 반응식
CO[C:3]1[C:8]([C:9]#[N:10])=[C:7]([CH3:11])[N:6]=[CH:5][CH:4]=1.P(Cl)(Cl)(Cl)(Cl)[Cl:13]>P(Cl)(Cl)(Cl)=O>[Cl:13][C:3]1[C:8]([C:9]#[N:10])=[C:7]([CH3:11])[N:6]=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24819Phosphorus pentachlorideHCID 534026054-Methoxy-2-methylpyridine-3-carbonitrile

생성물 1

HCID 67125855HCID 67125855, 화합물수율 34.2%

시약·촉매·용매 1

HCID 24813Phosphorus oxychloride용매

실험 절차

To 4-methoxy-2-methylnicotinonitrile (Tet 6222, 2006) (100 mg, 0.67 mmol) in phosphoryl chloride (2 mL) was added phosphorus pentachloride (156 mg, 0.75 mmol). The mixture was heated to reflux under nitrogen for 15 h. The reaction was quenched with ice, stirred for 10 min, then neutralised with NaHCO3 and extracted with EtOAc. The combined organic extracts were dried (Na2SO4), evaporated to dryness and purified by column chromatography (Si—PCC, gradient 0-50% EtOAc in cyclohexane). Product containing fractions were evaporated to give the title compound as a pale pink solid, (35 mg, 34%). 1H NMR δ (ppm) (CDCl3-d): 8.56 (1H, d, J=5.46 Hz), 7.32 (2H, d, J=5.46 Hz), 2.81 (3H, s).

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후처리

  1. temperatureThe mixture was heated
  2. temperatureto reflux under nitrogen for 15 h
  3. customThe reaction was quenched with ice
  4. extractionextracted with EtOAc
  5. dry with materialThe combined organic extracts were dried (Na2SO4)
  6. customevaporated to dryness
  7. custompurified by column chromatography (Si—PCC, gradient 0-50% EtOAc in cyclohexane)
  8. additionProduct containing fractions
  9. customwere evaporated

출처 및 근거

ORD 기록
ord-3b650df287da4de9ae6dadfbde7bae5f
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08653089B2

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