Dimethylformamide → 5-Formyl-2-(methylsulfanyl)benzonitrile

HRID 593503Notes

Reaction equation

HRID 593503 reaction equation
F[C:2]1[CH:3]=[CH:4][C:5]([CH:10]=[O:11])=[C:6]([CH:9]=1)C#N.C(=O)([O-])[O-].[K+].[K+].[CH3:18][S-:19].[Na+].C[N:22]([CH:24]=O)C>C(OCC)(=O)C>[CH:10]([C:5]1[CH:4]=[CH:3][C:2]([S:19][CH3:18])=[C:9]([CH:6]=1)[C:24]#[N:22])=[O:11]

Participants

6

Reactant 4

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 4378561Sodium methanethiolateHCID 202966885-Fluoro-2-formylbenzonitrile

Product 1

HCID 179666355-Formyl-2-(methylsulfanyl)benzonitrile

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

A flask is charged with 5-fluoro-2-formyl-benzonitrile (0.200 g, 1.34 mmol), potassium carbonate (0.371 g, 0.268 mmol), sodium thiomethoxide (0.142 g, 2.01 mmol) and DMF (20 mL). The mixture is stirred at room temperature for 10 min, then diluted with ethyl acetate and washed with water. The organic layer is dried over sodium sulfate and concentrated in vacuo to afford 5-formyl-2-methylsulfanyl-benzonitrile as a yellow color solid. 1H NMR (400 MHz, CDCl3) δ ppm 2.64 (s, 3H), 7.41 (d, J=8.3 Hz, 1H), 8.01 (dd, J=8.5, 1.9 Hz, 1H), 8.07 (d, J=1.8 Hz, 1H), 9.95 (s, 1H).

Workup

  1. washwashed with water
  2. dry with materialThe organic layer is dried over sodium sulfate
  3. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-0946a5bcb59f4608a7057b330157af5a
Source dataset
uspto-grants-2016_01
Patent number
US09242963B2

Reaction notes

Loading…