Dimethyl Sulfone → HCID 67997695, compound

HRID 1425969Notes

Reaction equation

HRID 1425969 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5](F)=[N:6][CH:7]=1.C[Si](C)(C)[N-][Si](C)(C)C.[Na+].[CH3:19][S:20]([CH3:23])(=[O:22])=[O:21]>O1CCCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:19][S:20]([CH3:23])(=[O:22])=[O:21])=[N:6][CH:7]=1

Participants

5

Conditions

Temperature
-17 °C

Procedure

5-Bromo-2-fluoro-pyridine (2.00 g) dissolved in tetrahydrofuran (20 mL) was added dropwise to a solution of sodium hexamethyldisilazide (2 mol/L in tetrahydrofuran, 28.5 mL) in tetrahydrofuran (20 mL) cooled to ca. −17° C. Dimethylsulfone (4.30 g) was added and stirring continued in the cooling bath for 1 h. The cooling bath was then removed and the solution was stirred at room temperature for one more h. Aqueous NH4Cl solution and brine were added and the resulting mixture was extracted with ethyl acetate. The combined extracts were dried (MgSO4) and the solvent was evaporated. The residue was treated with little ethyl acetate to precipitate the title compound. Yield: 1.73 g (63% of theory); LC (method 3): tR=2.01 min; Mass spectrum (ESI+): m/z=250/252 (Br) [M+H]+.

Workup

  1. customThe cooling bath was then removed
  2. stirringthe solution was stirred at room temperature for one more h
  3. additionAqueous NH4Cl solution and brine were added
  4. extractionthe resulting mixture was extracted with ethyl acetate
  5. dry with materialThe combined extracts were dried (MgSO4)
  6. customthe solvent was evaporated
  7. additionThe residue was treated with little ethyl acetate
  8. customto precipitate the title compound

Sources & evidence

ORD record
ord-d9bb245521ed461dbdcfcf58d0b9f976
Source dataset
uspto-grants-2015_01
Patent number
US08933072B2

Reaction notes

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