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Potassium Carbonate → 3-Fluoro-4'-propylbiphenyl

HRID 1406826
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HRID 1406826 반응식
[CH2:1]([C:4]1[CH:9]=[CH:8][C:7](Br)=[CH:6][CH:5]=1)[CH2:2][CH3:3].C(=O)([O-])[O-].[K+].[K+].[F:17][C:18]1[CH:19]=[C:20](B(O)O)[CH:21]=[CH:22][CH:23]=1>C1COCC1>[F:17][C:18]1[CH:19]=[C:20]([C:7]2[CH:8]=[CH:9][C:4]([CH2:1][CH2:2][CH3:3])=[CH:5][CH:6]=2)[CH:21]=[CH:22][CH:23]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 1363741-Bromo-4-propylbenzeneHCID 27339863-Fluorophenylboronic acid

생성물 1

HCID 185211083-Fluoro-4'-propylbiphenyl수율 82.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
60 °C

실험 절차

In a nitrogen atmosphere, a solution prepared by mixing 50.00 g of 4-propylbromobenzene, 0.87 g of tetrakis-triphenylphosphine palladium, 60 mL of an aqueous potassium carbonate solution (2 mol/L), and 150 mL of THF was heated to 60° C., and 35.14 g of 3-fluorophenylboronic acid was added to the solution over 20 minutes. After the resultant mixture was stirred at 60° C. for 3 hours, the mixture was allowed to cool, and an organic layer was separated by adding hexane. The organic layer was washed with saturated brine and dried by adding sodium sulfate, and then the solvent was distilled off under reduced pressure. As a result of purification by silica gel column chromatography, 44.32 g of 3-fluoro-1-(4-propylphenyl)benzene was produced.

후처리

  1. customIn a nitrogen atmosphere, a solution prepared
  2. temperatureto cool
  3. customan organic layer was separated
  4. additionby adding hexane
  5. washThe organic layer was washed with saturated brine
  6. customdried
  7. additionby adding sodium sulfate
  8. distillationthe solvent was distilled off under reduced pressure
  9. customAs a result of purification by silica gel column chromatography

출처 및 근거

ORD 기록
ord-4168fa2b6b7049a4848e4d0929345adb
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916718B2

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