Cesium carbonate → (NE,R)-N-[(3-bromophenyl)methylidene]-2-methylpropane-2-sulfinamide

HRID 2207682Notes

Reaction equation

HRID 2207682 reaction equation
[CH3:1][C:2]([S@:5]([NH2:7])=[O:6])([CH3:4])[CH3:3].C([O-])([O-])=O.[Cs+].[Cs+].[Br:14][C:15]1[CH:16]=[C:17]([CH:20]=[CH:21][CH:22]=1)[CH:18]=O>C(Cl)Cl>[Br:14][C:15]1[CH:16]=[C:17](/[CH:18]=[N:7]/[S@@:5]([C:2]([CH3:4])([CH3:3])[CH3:1])=[O:6])[CH:20]=[CH:21][CH:22]=1

Participants

5

Procedure

To a mixture of (R)-2-methylpropane-2-sulfinamide (2.4326 g, 20.07 mmol) and Cs2CO3 (9.81 g, 30.1 mmol) in DCM (50 mL) was added dropwise a solution of 3-bromobenzaldehyde (4.08 g, 22.08 mmol) in DCM (50 mL) over 10 min and the mixture stirred at ambient temperature for overnight. The reaction mixture was filtered through celite and the filter pad washed with DCM then with EtOAc. Filtrate was dried over MgSO4 and concentrated to give an oil which was purified by silica gel chromatography to give 2A (4.7626 g, 16.53 mmol, 82% yield) as an faint yellow colored oil. 1H NMR (500 MHz, CDCl3) δ 8.55 (s, 1H), 8.05 (t, J=1.8 Hz, 1H), 7.76 (dt, J=7.7, 1.2 Hz, 1H), 7.68-7.65 (m, 1H), 7.41-7.36 (m, 1H), 1.31-1.29 (m, 9H).

Workup

  1. filtrationThe reaction mixture was filtered through celite
  2. washthe filter pad washed with DCM
  3. dry with materialFiltrate was dried over MgSO4
  4. concentrationconcentrated
  5. customto give an oil which
  6. customwas purified by silica gel chromatography

Sources & evidence

ORD record
ord-2217495ac74a47fc874b27a00cdb7fe1
Source dataset
uspto-grants-2016_06
Patent number
US09376444B2

Reaction notes

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