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Sodium hydride → 2-bromo-2,2-difluoro-N-(4-fluoro-2-hydroxyphenyl)acetamide

HRID 403156
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HRID 403156 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[OH:9].[H-].[Na+].[Br:12][C:13]([F:20])([F:19])[C:14](OCC)=[O:15]>O1CCCC1>[Br:12][C:13]([F:20])([F:19])[C:14]([NH:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[OH:9])=[O:15]
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참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 69585Ethyl bromodifluoroacetateHCID 1857632-Amino-5-fluorophenol

생성물 1

HCID 668361432-bromo-2,2-difluoro-N-(4-fluoro-2-hydroxyphenyl)acetamide수율 105.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-15 °C

실험 절차

To 2-amino-5-fluorophenol (14 g, 110 mmol) in dry tetrahydrofuran at 0° C. was added sodium hydride (55 wt % in mineral oil; 4.81 g, 110 mmol). The resulting mixture was stirred for 15 minutes at −15° C. Subsequently ethyl 2-bromo-2,2-difluoroacetate (24.59 g, 121 mmol) was added dropwise and the resulting mixture was stirred at 0° C. for two hours. The reaction mixture was quenched with saturated aqueous NH4Cl solution and extracted with ethyl acetate. The combined extracts were washed with brine, dried with Na2SO4 and concentrated to yield 33 g of the title compound.

후처리

  1. stirringthe resulting mixture was stirred at 0° C. for two hours
  2. customThe reaction mixture was quenched with saturated aqueous NH4Cl solution
  3. extractionextracted with ethyl acetate
  4. washThe combined extracts were washed with brine
  5. dry with materialdried with Na2SO4
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2e802e5e75954c5ebb0b7d30ac99fcd4
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08748348B2

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