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Sodium Carbonate → 2-(3,5-Difluoro-4'-propylbiphenyl-4-yl)-5-methylthiophene

HRID 449732
ノート
印刷プレビュー

反応式

HRID 449732 の反応式
Br[C:2]1[S:3][C:4]([CH3:7])=[CH:5][CH:6]=1.[CH2:8]([C:11]1[CH:16]=[CH:15][C:14]([C:17]2[CH:22]=[C:21]([F:23])[C:20](B(O)O)=[C:19]([F:27])[CH:18]=2)=[CH:13][CH:12]=1)[CH2:9][CH3:10].C(=O)([O-])[O-].[Na+].[Na+]>C1(C)C=CC=CC=1.C(O)C.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[F:23][C:21]1[CH:22]=[C:17]([C:14]2[CH:15]=[CH:16][C:11]([CH2:8][CH2:9][CH3:10])=[CH:12][CH:13]=2)[CH:18]=[C:19]([F:27])[C:20]=1[C:2]1[S:3][C:4]([CH3:7])=[CH:5][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 10340Sodium CarbonateHCID 698312-Bromo-5-methylthiopheneHCID 580284314'-Propyl-3,5-difluoro-4-biphenylboronic acid

生成物 1

HCID 580284522-(3,5-Difluoro-4'-propylbiphenyl-4-yl)-5-methylthiophene

試薬・触媒・溶媒 2

HCID 178418397HCID 178418397、化合物触媒
HCID 21863594
Toluene ethanol
溶媒

実験手順

A mixture of 5.50 g (31.0 mmol) of 2-bromo-5-methylthiophene, 9.0 g (32.6 mmol) of 4′-propyl-3,5-difluoro-4-biphenylboronic acid, 1.83 g (1.58 mmol) of tetrakis(triphenylphosphine)palladium(0) and 36 ml of 2 N sodium carbonate soln. in 90 ml of toluene/ethanol (1:2) is heated under reflux for 16 h. After cooling, the organic phase is separated off, and the aqueous phase is extracted a number of times with toluene. The combined organic phases are washed with water and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to completion. The residue is purified by column chromatography (SiO2, n-heptane:toluene=9:1). Further purification is carried out by recrystallisation from ethanol and n-heptane; 2-(3,5-difluoro-4′-propylbiphenyl-4-yl)-5-methylthiophene (PUS-3-1) is obtained as a colourless solid (m.p. 75° C.).

後処理

  1. temperatureunder reflux for 16 h
  2. temperatureAfter cooling
  3. customthe organic phase is separated off
  4. extractionthe aqueous phase is extracted a number of times with toluene
  5. washThe combined organic phases are washed with water and sat. sodium chloride soln
  6. customThe solution is dried
  7. concentrationconcentrated to completion
  8. customThe residue is purified by column chromatography (SiO2, n-heptane:toluene=9:1)
  9. customFurther purification
  10. customis carried out by recrystallisation from ethanol and n-heptane

出典と根拠

ORDレコード
ord-8d5c3e19b21040d981c448917de5348d
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08486297B2

反応ノート

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