Water → HCID 17989159, compound

HRID 1444395Notes

Reaction equation

HRID 1444395 reaction equation
F[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[O:9][CH3:10].C[Si](C)(C)[N-:13][Si](C)(C)C.[K+].O.S(=O)(=O)(O)O.[C:27]1([CH3:33])[CH:32]=CC=C[CH:28]=1>C(OCC)(=O)C>[F:8][C:4]1[C:3]([O:9][CH3:10])=[C:2]([C:27]([CH3:33])([CH3:32])[C:28]#[N:13])[CH:7]=[CH:6][CH:5]=1

Participants

7

Procedure

10 g (69.39 mol) of 2,6-difluoroanisole is dissolved in 200 ml of toluene and mixed at room temperature with 5.75 g (83.27 mmol) of isobutyric acid nitrile. 166.5 ml of a 0.5 molar solution of potassium hexamethyldisilazide in toluene is added in drops within 35 minutes. In this case, a slight temperature rise to 27.5° C. takes place. After 16 hours of stirring at room temperature, the reaction mixture is mixed with 200 ml of water and 400 ml of ethyl acetate and acidified with 10% sulfuric acid to a pH of 4. The organic phase is separated, and the aqueous phase is shaken once with ethyl acetate (200 ml). The combined organic extracts are shaken with water and brine. After the solvent is dried, filtered and spun off, the residue is chromatographed on silica gel (mobile solvent ethyl acetate/hexane). 7.66 g (57.1%) of the desired compound is isolated.

Workup

  1. customto 27.5° C.
  2. customThe organic phase is separated
  3. stirringthe aqueous phase is shaken once with ethyl acetate (200 ml)
  4. stirringThe combined organic extracts are shaken with water and brine
  5. customAfter the solvent is dried
  6. filtrationfiltered
  7. customthe residue is chromatographed on silica gel (mobile solvent ethyl acetate/hexane)

Sources & evidence

ORD record
ord-c68d2a2a45784703b18fddca2c29c9fe
Source dataset
uspto-grants-2010_02
Patent number
US07662821B2

Reaction notes

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