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Phosphorus oxychloride → 6-Bromo-4-chloro-3-phenyl-2-(trifluoromethyl)quinoline

HRID 627503
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HRID 627503 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([C:12]([F:15])([F:14])[F:13])[C:6]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[C:5]2O.P(Cl)(Cl)([Cl:25])=O>>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([C:12]([F:15])([F:14])[F:13])[C:6]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[C:5]2[Cl:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178515323HCID 178515323, 화합물

생성물 1

HCID 867160766-Bromo-4-chloro-3-phenyl-2-(trifluoromethyl)quinoline

실험 절차

A solution of 6-bromo-3-phenyl-2-(trifluoromethyl)quinolin-4-ol (8.29 g, 22.5 mmol, Intermediate 34, step a) in phosphoryl trichloride (25 mL, 269 mmol) was heated at 110° C. for 2 hours, and concentrated in vacuo. Dichloromethane and ice-water were added, and the mixture was basified at 4° C. with conc. NH4OH until pH ˜10. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined organic phases were dried (Na2SO4), filtered, concentrated, and purified by flash column chromatography (120 g silica gel column, 2-9% EtOAc in heptane) to give the title compound as a light yellow solid.

후처리

  1. concentrationconcentrated in vacuo
  2. additionDichloromethane and ice-water were added
  3. custom
was basified at 4° C. with conc. NH4OH until pH ˜10
  • customThe organic layer was separated
  • extractionthe aqueous layer was extracted with CH2Cl2
  • dry with materialThe combined organic phases were dried (Na2SO4)
  • filtrationfiltered
  • concentrationconcentrated
  • custompurified by flash column chromatography (120 g silica gel column, 2-9% EtOAc in heptane)
  • 출처 및 근거

    ORD 기록
    ord-44cf13aae3ed445ea7dd95b192a36258
    출처 데이터셋
    uspto-grants-2016_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09309222B2

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