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Ammonium Chloride → (5-Bromo-2,4-difluoro-phenyl)-(3-fluoro-phenyl)-methanol

HRID 1610118
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HRID 1610118 반응식
Br[C:2]1[CH:7]=[C:6]([Br:8])[C:5]([F:9])=[CH:4][C:3]=1[F:10].C([Li])CCC.[F:16][C:17]1[CH:18]=[C:19]([CH:22]=[CH:23][CH:24]=1)[CH:20]=[O:21].[Cl-].[NH4+]>C(OCC)C.CCCCCC>[Br:8][C:6]1[C:5]([F:9])=[CH:4][C:3]([F:10])=[C:2]([CH:20]([C:19]2[CH:22]=[CH:23][CH:24]=[C:17]([F:16])[CH:18]=2)[OH:21])[CH:7]=1
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참가 물질

7

반응물 4

HCID 25517Ammonium ChlorideHCID 680093-FluorobenzaldehydeHCID 105645111,5-Dibromo-2,4-difluorobenzeneHCID 178418339Butyllithium

생성물 1

HCID 22260768(5-Bromo-2,4-difluoro-phenyl)-(3-fluoro-phenyl)-methanol

시약·촉매·용매 2

HCID 3283Diethyl Ether용매
HCID 8058
Hexane
용매

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온도
-70 °C

실험 절차

A total of 2.02 g of 1,5-dibromo-2,4-difluorobenzene obtained in Production Example II-5-a was dissolved in 38 ml of diethyl ether, and 4.9 ml of a 1.58 M solution of n-butyllithium in hexane was added under stirring at −70° C. After stirring for 1 hour, 4.9ml of m-fluorobenzaldehyde was added and the mixture was stirred for 15 minutes. Saturated aqueous ammonium chloride solution was added to the reaction mixture, followed by extracting with ethyl acetate. The resulting organic layer was washed with brine, dried over magnesium sulfate and the solvent was evaporated. The residue was purified and separated by silica gel column chromatography (ethyl acetate:hexane=1:10), to give 0.96 g of the title compound.

후처리

  1. stirringAfter stirring for 1 hour
  2. stirringthe mixture was stirred for 15 minutes
  3. extractionby extracting with ethyl acetate
  4. washThe resulting organic layer was washed with brine
  5. dry with materialdried over magnesium sulfate
  6. customthe solvent was evaporated
  7. customThe residue was purified
  8. customseparated by silica gel column chromatography (ethyl acetate:hexane=1:10)

출처 및 근거

ORD 기록
ord-11bdcb7cda4348c889ed6635c82061dd
출처 데이터셋
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06982274B2

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