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Water → 3'-Fluoro-4'-methylbiphenyl-2-carboxylic acid t-butyl ester

HRID 475668
ノート
印刷プレビュー

反応式

HRID 475668 の反応式
[C:1]([O:5][C:6](=[O:14])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1Br)([CH3:4])([CH3:3])[CH3:2].[F:15][C:16]1[CH:17]=[C:18](B(O)O)[CH:19]=[CH:20][C:21]=1[CH3:22].C(O)(C)C.C(=O)([O-])[O-].[Na+].[Na+].O>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>[C:1]([O:5][C:6]([C:7]1[C:8]([C:18]2[CH:19]=[CH:20][C:21]([CH3:22])=[C:16]([F:15])[CH:17]=2)=[CH:9][CH:10]=[CH:11][CH:12]=1)=[O:14])([CH3:4])([CH3:3])[CH3:2]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 962WaterHCID 3776IsopropanolHCID 10340Sodium CarbonateHCID 27826743-Fluoro-4-methylbenzeneboronic acidHCID 3804415tert-Butyl 2-bromobenzoate

生成物 1

HCID 574839403'-Fluoro-4'-methylbiphenyl-2-carboxylic acid t-butyl ester収率 76.6%

試薬・触媒・溶媒 1

HCID 178418397HCID 178418397、化合物触媒

反応条件

温度
90 °C

実験手順

Compound A (80.0 g, 311 mmol) and 3-fluoro-4-methylphenylboronic acid (52.7 g, 342 mmol) were suspended in isopropyl alcohol (260 mL, 3.5 mol). A solution of sodium carbonate (56.1 g, 529 mmol) in water (260 mL, 15 mol) was added and the mixture was degassed under nitrogen. Tetrakis(triphenylphosphine)palladium(0) (3.6 g, 3.1 mmol) was then added and the mixture was stirred at 90° C. for 17 hours. The mixture was concentrated under reduced pressure and suspended in water (200 mL). The aqueous phase was extracted with EtOAc (600 mL) and separated. The organic phase was washed with saturated aqueous NaCl and concentrated under reduced pressure. The recovered oil was purified by silica gel chromatography (4-6% 5×120 g column) to yield compound B as a clear oil (68.2 g).

後処理

  1. customthe mixture was degassed under nitrogen
  2. concentrationThe mixture was concentrated under reduced pressure
  3. extractionThe aqueous phase was extracted with EtOAc (600 mL)
  4. customseparated
  5. washThe organic phase was washed with saturated aqueous NaCl
  6. concentrationconcentrated under reduced pressure
  7. customThe recovered oil was purified by silica gel chromatography (4-6% 5×120 g column)

出典と根拠

ORDレコード
ord-42eba26a4feb4aff94b1503ef8fed07e
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08637562B2

反応ノート

読み込み中…

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