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2-Bromo-5-fluorobenzonitrile → 5'-Acetyl-4,2'-difluorobiphenyl-2-carbonitrile

HRID 1064264
ノート
印刷プレビュー

反応式

HRID 1064264 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][C:3]=1B1OC(C)(C)C(C)(C)O1.Br[C:21]1[CH:28]=[CH:27][C:26]([F:29])=[CH:25][C:22]=1[C:23]#[N:24].[F-].[K+]>C1COCC1.O.C(Cl)Cl.C(P(C(C)(C)C)C(C)(C)C)(C)(C)C>[C:8]([C:5]1[CH:6]=[CH:7][C:2]([F:1])=[C:3]([C:21]2[C:22]([C:23]#[N:24])=[CH:25][C:26]([F:29])=[CH:27][CH:28]=2)[CH:4]=1)(=[O:10])[CH3:9]
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

8

反応物 3

HCID 936542-Bromo-5-fluorobenzonitrileHCID 522689Potassium FluorideHCID 222735921-(4-Fluoro-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethan-1-one

生成物 1

HCID 222735995'-Acetyl-4,2'-difluorobiphenyl-2-carbonitrile収率 58.2%

試薬・触媒・溶媒 4

HCID 83681Tris(1,1-dimethylethyl)phosphine触媒
HCID 962
Water
溶媒
HCID 6344Dichloromethane溶媒
HCID 8028Tetrahydrofuran溶媒

反応条件

温度
70 °C

実験手順

To a degassed solution of 1-[4-fluoro-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]ethanone (12 g, 45.43 mmol), 2-bromo-5-fluorobenzonitrile (9.09 g, 5.28 ml, 45.44 mmol), potassium fluoride (7.92 g, 136.31 mmol) and tris(dibenzylideneacetone)palladium(0) (0.834 g, 0.908 mmol) in THF (200 ml) and water (10 ml) was added tri-tert butylphosphine (10% weight solution) (0.368 g, 3.63 ml, 1.817 mmol). The reaction was heated at 70° C. for 14 h then allowed to cool to ambient temperature. The reaction was partitioned between water (200 ml) and ether (300 ml). The aqueous phase was extracted with ether (150 ml) and the combined organics washed with brine (200 ml), dried (MgSO4), filtered and evaporated to give a brown solid. The solid was dissolved in DCM and adsorbed onto silica. The crude product was chromatographed on silica (5-20% EtOAc in isohexane) to give the title product as a white solid (6.8 g): δH (400 MHz, CDCl3) 2.63 (3H, s), 7.31 (1H, t, J 9.0 Hz), 7.40-7.44 (1H, m), 7.50-7.53 (2H, m), 8.02-8.10 (2H, m).

後処理

  1. temperatureto cool to ambient temperature
  2. customThe reaction was partitioned between water (200 ml) and ether (300 ml)
  3. extractionThe aqueous phase was extracted with ether (150 ml)
  4. washthe combined organics washed with brine (200 ml)
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. customevaporated
  8. customto give a brown solid
  9. customThe crude product was chromatographed on silica (5-20% EtOAc in isohexane)

出典と根拠

ORDレコード
ord-13bb162f9eca4037acf08c41805da85d
出典データセット
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06969716B2

反応ノート

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