Potassium Carbonate → HCID 15058629, compound

HRID 452292Notes

Reaction equation

HRID 452292 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([OH:9])[CH:6]=[CH:7][CH:8]=1)#[N:2].C(=O)([O-])[O-].[K+].[K+].Br[CH2:17][CH2:18][F:19]>[I-].[K+].CS(C)=O>[F:19][CH2:18][CH2:17][O:9][C:5]1[CH:4]=[C:3]([CH:8]=[CH:7][CH:6]=1)[C:1]#[N:2]

Participants

6

Procedure

To a flame dried 50 mL round bottom flask was added 3-cyanophenol (1.0 g, 8.39 mmol) followed by 10 mL dimethyl sulfoxide. Potassium iodide (7.0 mg, 0.042 mmol) and potassium carbonate (1.74 g, 12.6 mmol) were added. The flask was immersed in an oil bath at 85° C. and 1-bromo-2-fluoroethane (1.17 g, 0.686 mL, 9.23 mmol) was added. The reaction was stirred at this temperature for 30 min, cooled to room temperature, filtered, and the filtrate was diluted with water (100 mL). The resulting solution was extracted with dichloromethane (3×30 mL). The organic layer was then washed with water (5×20 mL) and brine, and dried over magnesium sulfate. The solution was filtered and concentrated in vacuo to obtain 1.31 g (94%) of an oil as the product. 1H NMR (600 MHz, CDCl3): δ 7.37 (m, 1H), 7.26 (m, 1H), 7.15 (m, 2H), 4.75 (t of d, 2H, J=4.2, 46.8 Hz), 4.22 (t of d, 2H, J=4.2, 27.6 Hz). 13C NMR (75 MHz, CDCl3): δ 158.4, 130.4, 125, 119.8, 117.9, 117.5, 113.3, 81 (d, J=171 Hz), 67.4 (d, J=10.1 Hz).

Workup

  1. customTo a flame dried 50 mL round bottom flask
  2. customThe flask was immersed in an oil bath at 85° C.
  3. filtrationfiltered
  4. additionthe filtrate was diluted with water (100 mL)
  5. extractionThe resulting solution was extracted with dichloromethane (3×30 mL)
  6. washThe organic layer was then washed with water (5×20 mL) and brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationThe solution was filtered
  9. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-5450d4baba7f4729ab8f7bf32569d67a
Source dataset
uspto-grants-2013_07
Patent number
US08491868B2

Reaction notes

Loading…