(4-Fluorophenyl)dimethylphosphine oxide → 1-(Dimethyl-phosphinoyl)-4-nitro-benzene

HRID 50624Notes

Reaction equation

HRID 50624 reaction equation
[CH3:1][P:2]([CH3:11])([C:4]1[CH:9]=[CH:8][C:7](F)=[CH:6][CH:5]=1)=[O:3].[Li][N+:13]([O-:15])=[O:14]>CN1C(=O)N(C)CCC1.[Cl-].[Na+].O.CC(O)C>[CH3:1][P:2]([CH3:11])([C:4]1[CH:9]=[CH:8][C:7]([N+:13]([O-:15])=[O:14])=[CH:6][CH:5]=1)=[O:3]

Participants

6

Reactant 2

HCID 21897903(4-Fluorophenyl)dimethylphosphine oxideHCID 178506934HCID 178506934, compound

Product 1

HCID 218979121-(Dimethyl-phosphinoyl)-4-nitro-benzeneYield 45.1%

Reagents, catalysts & solvents 3

HCID 3776IsopropanolSolventHCID 816462(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-SolventHCID 57417360Sodium chloride; waterSolvent

Procedure

A sealed pressure flask, flushed with N2, containing a mixture of 3.90 g (22.7 mmol) of 1-(Dimethyl-phosphinoyl)-4-fluoro-benzene and 6.0 g (113.3 mmol) of LiNO2 (for prep see, W. C. Ball and H. H. Abram J. Chem. Soc. 1913, 103, 2130-2134) in 27 mL of DMPU (1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone) was stirred at ambient temperature for 5-10 min (to dissolve fluoro compound) then heated at 190° C. for 3 days. The resulting dark brown solution was cooled to ambient temperature, diluted with 300 mL of brine, then extracted with EtOAc (10×100 mL) until the aqueous layer showed little or no evidence of product by HPLC. The combined organics were dried over MgSO4 and concentrated. The excess DMPU was removed via short-path distillation (120° C./0.3 mm) to provide a semi-solid, which was dissolved in a minimum amount of iPrOH and purified by silica gel flash chromatography (eluted with 5% iPrOH/DCM, then 10% iPrOH/DCM, then 15% iPrOH/DCM) to provide 2.04 g of an yellow solid: 1H NMR (300 MHz, DMSO-d6) δ8.34 (dd, J=8.7, 1.9 Hz, 2H), 8.07 (dd, J=10.6, 8.8 Hz, 2H), 1.75 (s, 3H), 1.70 (s, 3H). 31P NMR (121 MHz, DMSO-d6) δ37.89.

Workup

  1. customA sealed pressure flask, flushed with N2
  2. additioncontaining
  3. temperaturethen heated at 190° C. for 3 days
  4. temperatureThe resulting dark brown solution was cooled to ambient temperature
  5. extractionextracted with EtOAc (10×100 mL) until the aqueous layer
  6. dry with materialThe combined organics were dried over MgSO4
  7. concentrationconcentrated
  8. customThe excess DMPU was removed via short-path distillation (120° C./0.3 mm)
  9. customto provide a semi-solid, which
  10. custompurified by silica gel flash chromatography (
  11. washeluted with 5% iPrOH/DCM

Sources & evidence

ORD record
ord-bf9184ac45334d598d4f04d6f1e9bb88
Source dataset
uspto-grants-2004_03
Patent number
US06713462B2

Reaction notes

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