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Water → HCID 89825734, 화합물

HRID 1775374
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HRID 1775374 반응식
[Br:1][C:2]1[CH:7]=[C:6]([O:8][CH2:9][CH3:10])[CH:5]=[C:4]([CH3:11])[N+:3]=1[O-].P(Cl)(Cl)Cl.O.C(#N)C>C(OCC)(=O)C>[Br:1][C:2]1[CH:7]=[C:6]([O:8][CH2:9][CH3:10])[CH:5]=[C:4]([CH3:11])[N:3]=1
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참가 물질

6

반응물 4

HCID 962WaterHCID 6342AcetonitrileHCID 24387Phosphorus trichlorideHCID 89826007HCID 89826007, 화합물

생성물 1

HCID 89825734HCID 89825734, 화합물수율 24%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매2회

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온도
50 °C

실험 절차

2-Bromo-6-methyl-4-ethoxy-pyridine 1-oxide (a total of 9.85 g, 42 mmol) was divided in two batches, suspended in ethyl acetate (anhydrous, total of 130 ml), phosphorus trichloride (total of 15 ml) was added dropwise and the mixtures were stirred at 50° C. for three hours. Then the mixture of each batch was poured onto crushed ice (250 ml each) with stirring, ethyl acetate (250 ml each) was added, the phases were separated and the organic phases were washed with water (2 times), dried (magnesium sulfate) and concentrated under reduced pressure. The residues were combined and purified by column chromatography (silica, petrolether/ethyl acetate 95:5) and then by preparative HPLC (Waters XBridge, gradient of water containing 0.1% NH3 and acetonitrile) to give 2.2 g of a yellow oil (10 mmol, 24% yield).

후처리

  1. additionThen the mixture of each batch
  2. additionwas poured
  3. stirringwith stirring
  4. customthe phases were separated
  5. washthe organic phases were washed with water (2 times)
  6. dry with materialdried (magnesium sulfate)
  7. concentrationconcentrated under reduced pressure
  8. custompurified by column chromatography (silica, petrolether/ethyl acetate 95:5)

출처 및 근거

ORD 기록
ord-91859777ad144681bcf0a78a7caff442
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09260441B2

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