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Iodine → 1-Phenyl-2-pyridin-4-ylethane-1,2-dione

HRID 271112
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HRID 271112 반응식
[C:1]1([C:7]#[C:8][C:9]2[CH:14]=[CH:13][N:12]=[CH:11][CH:10]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.II.[OH2:17].C([O-])([O-])=[O:19].[Na+].[Na+]>CS(C)=O>[C:1]1([C:7](=[O:19])[C:8]([C:9]2[CH:10]=[CH:11][N:12]=[CH:13][CH:14]=2)=[O:17])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
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참가 물질

6

반응물 4

HCID 807IodineHCID 962WaterHCID 10340Sodium CarbonateHCID 3521724-(Phenylethynyl)pyridine

생성물 1

HCID 2750111-Phenyl-2-pyridin-4-ylethane-1,2-dione수율 30%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

A solution of 4-(phenylethynyl)pyridine (2.25 g, 12.6 mmol) and powder iodine (1.60 g, 6.3 mmol) in DMSO (30 mL) is heated at 155° C. for 4 h. The reaction mixture is cooled and poured to H2O (100 mL). The aqueous is neutralized with powdered Na2CO3 to pH˜12 and extracted with EtOAc (2×100 mL). The combined organic extracts are washed sequentially with H2O (60 mL) and brine (60 mL), then dried and concentrated. The crude material is purified by chromatography (silica gel: EtOAc/hexane: 20/80) to afford the title compound (0.81 g, 30%) as an oil. MS (+) ES: 212 (M+H)+.

후처리

  1. temperatureThe reaction mixture is cooled
  2. extractionextracted with EtOAc (2×100 mL)
  3. washThe combined organic extracts are washed sequentially with H2O (60 mL) and brine (60 mL)
  4. customdried
  5. concentrationconcentrated
  6. customThe crude material is purified by chromatography (silica gel: EtOAc/hexane: 20/80)

출처 및 근거

ORD 기록
ord-32057cbc368447d8ace7b862dde589a0
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07452885B2

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