Potassium Carbonate → HCID 24695760, compound

HRID 1476761Notes

Reaction equation

HRID 1476761 reaction equation
Br[CH2:2][CH2:3][O:4][CH3:5].[Br:6][C:7]1[CH:12]=[C:11]([F:13])[CH:10]=[CH:9][C:8]=1[OH:14].C([O-])([O-])=O.[K+].[K+]>CC#N>[Br:6][C:7]1[CH:12]=[C:11]([F:13])[CH:10]=[CH:9][C:8]=1[O:14][CH2:2][CH2:3][O:4][CH3:5]

Participants

5

Conditions

Temperature
80 °C

Procedure

1-bromo-2-methoxyethane (5.49 g, 39.5 mmol) was added to a mixture of 2-bromo-4-fluoro phenol (5 g, 26.18 mmol) and K2CO3 (11.5 g, 83.25 mmol) in CH3CN (41.5 mL) and continued stirring at 80° C. for 16 hr. The reaction mixture was quenched with 1M aq.NaOH solution, extracted with diethyl ether (3×100 mL), dried over anhydrous sodium sulphate and concentrated under reduced pressure to afford the crude, which was purified by column chromatography (using silica gel and 2% ethyl acetate in hexane as eluent) to afford the desired compound (Int-42). 1H NMR (300 MHz, CDCl3) δ ppm 7.3 (1H, m), 6.9 (1H, m), 6.7 (1H, m), 4.1 (2H, t), 3.8 (2H, t), 3.5 (3H, s).

Workup

  1. customThe reaction mixture was quenched with 1M aq
  2. extractionNaOH solution, extracted with diethyl ether (3×100 mL)
  3. dry with materialdried over anhydrous sodium sulphate
  4. concentrationconcentrated under reduced pressure
  5. customto afford the crude, which
  6. customwas purified by column chromatography (using silica gel and 2% ethyl acetate in hexane as eluent)

Sources & evidence

ORD record
ord-a7adbb57ebae4983837159bbc90c1b01
Source dataset
uspto-grants-2016_08
Patent number
US09402833B2

Reaction notes

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