Bromine → 1-Bromo-1-(methylsulfonyl)-2-propanone

HRID 220370

Reaction equation

HRID 220370 reaction equation
[CH3:1][S:2]([CH2:5][C:6](=[O:8])[CH3:7])(=[O:4])=[O:3].[Br:9]Br>CC(O)=O.ClCCl>[Br:9][CH:5]([S:2]([CH3:1])(=[O:4])=[O:3])[C:6](=[O:8])[CH3:7]

Participants

5

Procedure

To a solution of methanesulphonylacetone (0.5 g, 3.67 mmol) in AcOH (7.34 mL) and dichloromethane (11.02 mL) in a round bottom flask was added bromine (0.189 mL, 3.67 mmol) dropwise. The reaction mixture was stirred at rt 90 min. Solvent was removed in vacuo. The residue was taken up in ether and washed with saturated aqueous sodium bicarbonate (2×). The organics were concentrated in vacuo. 1-Bromo-1-(methylsulfonyl)propan-2-one (0.332 g, 42% yield) was isolated as an oil.

Workup

  1. customSolvent was removed in vacuo
  2. washwashed with saturated aqueous sodium bicarbonate (2×)
  3. concentrationThe organics were concentrated in vacuo

Sources & evidence

ORD record
ord-d904e2e21c024f3489eba3c9a23001ad
Source dataset
uspto-grants-2012_06
Patent number
US08202881B2

Linked notes

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