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Ethyl difluoroacetate → 2,2-Difluoro-1-(2-fluoro-4-methoxyphenyl)ethan-1-one

HRID 216337
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HRID 216337 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[F:10].[Li]CCCC.[F:16][CH:17]([F:23])[C:18](OCC)=[O:19]>CCOCC>[F:16][CH:17]([F:23])[C:18]([C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[F:10])=[O:19]
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참가 물질

5

반응물 3

HCID 9961Ethyl difluoroacetateHCID 37184441-Bromo-2-fluoro-4-methoxybenzeneHCID 178418339Butyllithium

생성물 1

HCID 866384912,2-Difluoro-1-(2-fluoro-4-methoxyphenyl)ethan-1-one

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
-78 °C

실험 절차

To 1-bromo-2-fluoro-4-methoxybenzene (123 g, 0.6 mol) in 1300 mL Et2O at −78° C. was added n-BuLi (276 mL, 2.5 M) dropwise. After stirring at −78° C. for 2 hours, ethyl difluoroacetate (82.6 g, 0.67 mol) was added dropwise at −78° C. The reaction was stirred overnight at 25° C., and was quenched with saturated ammonium chloride solution at −20° C., followed by 1N HCl (final pH=4). The organic layer was separated and aqueous layer was extracted with Et2O. The combined extracts were dried over MgSO4, filtered and concentrated, and the residue was purified by column chromatography (PE/EA 20:1) to afford 2,2-difluoro-1-(2-fluoro-4-methoxyphenyl)ethanone as an oil.

후처리

  1. stirringThe reaction was stirred overnight at 25° C.
  2. customwas quenched with saturated ammonium chloride solution at −20° C.
  3. customThe organic layer was separated
  4. extractionaqueous layer was extracted with Et2O
  5. dry with materialThe combined extracts were dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customthe residue was purified by column chromatography (PE/EA 20:1)

출처 및 근거

ORD 기록
ord-7e606834702e46d0bb50c2892372d5be
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08193228B2

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