Hydrochloric Acid → 4-Acetyl-2-fluorobenzonitrile

HRID 984803

反応式

HRID 984803 の反応式
Br[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([F:10])[CH:3]=1.C1C=CC(P(C2C=CC=[CH:38][CH:39]=2)CCCP(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.N#N.Cl.CN(C=[O:47])C>CC([O-])=O.CC([O-])=O.[Pd+2].O>[C:38]([C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([F:10])[CH:3]=1)(=[O:47])[CH3:39]

参加物

8

反応条件

温度
90 °C

実験手順

A mixture of 5.0 g (0.02 mol) 4-bromo-2-fluorobenzonitrile, 6 ml TEA, 906 mg (0.0022 mol) dppp, 5.8 g (0.04 mol) TIOAc, and 448 mg (0.002 mol) Pd(OAc)2 in 50 ml DMF was deaired under a stream of N2. The mixture was heated to 90° C. for 7 hours. The reaction was cooled to room temperature and 25 mL 2N HCl was added and stirred to 30 minutes. The mixture was poured into 300 ml water and extracted with Et2O (2×300 mL). The combined organics were washed with water (2×80 mL), brine (1×80 mL), dried over MgSO4 and concentrated to give an oil, which was then chromatographed on silica gel eluted with 30% ethyl acetate/70% hexanes to give 2.5 g of a yellow/orange oil.

後処理

  1. temperatureThe reaction was cooled to room temperature
  2. extractionextracted with Et2O (2×300 mL)
  3. washThe combined organics were washed with water (2×80 mL), brine (1×80 mL)
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. customto give an oil, which
  7. customwas then chromatographed on silica gel
  8. washeluted with 30% ethyl acetate/70% hexanes

出典と根拠

ORDレコード
ord-2f1a1e388a874a98b60d51f94cf136bd
出典データセット
uspto-grants-2005_03
特許番号
US06869945B2

関連ノート

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