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Phosphorus oxychloride → 2-Chloro-3-nitro-5-(2-methylpropyl)pyridine

HRID 722054
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인쇄 미리보기

반응식

HRID 722054 반응식
O[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:5]([CH2:11][CH:12]([CH3:14])[CH3:13])=[CH:4][N:3]=1.P(Cl)(Cl)([Cl:17])=O.[Na].C(=O)([O-])O>>[Cl:17][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:5]([CH2:11][CH:12]([CH3:14])[CH3:13])=[CH:4][N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 24813Phosphorus oxychlorideHCID 50987224Sodium hydrogen-carbonateHCID 1784413372-Hydroxy-3-nitro-5-(2-methylpropyl)pyridine2회

생성물 1

HCID 218827262-Chloro-3-nitro-5-(2-methylpropyl)pyridine

반응 조건

온도
120 °C

실험 절차

A mixture of 1.7 g of 2-hydroxy-3-nitro-5-(2-methylpropyl)pyridine (starting material D4) and 15 ml of phosphorous oxychloride is heated under reflux to 120° C. for two hours. After cooling the mixture is carefully added to ice/water, then neutralized with sodium-hydrogencarbonate and extracted three times with ethylacetate. The combined organic phases are evaporated to dryness and the residue is chromatographed on a silica gel column (ethylacetate/petroleum ether 1:15). Concentration of the chromatographically pure fractions gives 1.17 g of the title compound as an orange oil.

후처리

  1. temperatureis heated
  2. temperatureAfter cooling the mixture
  3. extractionextracted three times with ethylacetate
  4. customThe combined organic phases are evaporated to dryness
  5. customthe residue is chromatographed on a silica gel column (ethylacetate/petroleum ether 1:15)

출처 및 근거

ORD 기록
ord-bf5a6deaea9f441fb5f3f6c70fa43b82
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07138399B2

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