Phosphorus oxychloride → HCID 86648182, compound

HRID 574946Notes

Reaction equation

HRID 574946 reaction equation
O=P(Cl)(Cl)Cl.C[N+](C)=[CH:8][Cl:9].[Cl-].[F:12][CH2:13][C:14]1([CH2:21][F:22])[CH2:19][CH2:18][C:17](=[O:20])[CH2:16][CH2:15]1.C([O-])(O)=O.[Na+]>ClCCl.CN(C)C=O>[Cl:9][C:8]1[CH2:18][CH2:19][C:14]([CH2:21][F:22])([CH2:13][F:12])[CH2:15][C:16]=1[CH:17]=[O:20]

Participants

7

Conditions

Temperature
0 °C

Procedure

To a 100 mL pear flask was added N,N-dimethylformamide (498 μl) and dichloromethane (8.9 mL) to give a colorless solution. The solution was cooled to 0° C. and POCl3 (550 μl) was added dropwise and then the mixture was warmed to room temperature for 30 minutes. In the meantime, to a 100 mL pear shaped flask was added EXAMPLE 353C (870 mg, 5.36 mmol) in dichloromethane (8941 μl) to give a colorless solution. The Vilsmeier reagent was then taken up in a syringe and added dropwise to the 4,4-bis(fluoromethyl)cyclohexanone (870 mg) solution at room temperature. The resulting solution was stirred overnight. The reaction was poured into saturated aqueous NaHCO3 and ice, warmed to room temperature and extracted with dichloromethane (3×30 mL). The organics were combined, dried over MgSO4, filtered and concentrated by rotary evaporation. The residue was purified by regular phase flash column chromatography (Analogix (0-60% hexanes/ethyl acetate).

Workup

  1. customto give a colorless solution
  2. temperaturethe mixture was warmed to room temperature for 30 minutes
  3. customto give a colorless solution
  4. temperaturewarmed to room temperature
  5. extractionextracted with dichloromethane (3×30 mL)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated by rotary evaporation
  9. customThe residue was purified by regular phase flash column chromatography (Analogix (0-60% hexanes/ethyl acetate)

Sources & evidence

ORD record
ord-4bd53d11cb7e4d92b7b590b0ea5145b8
Source dataset
uspto-grants-2015_05
Patent number
US09034875B2

Reaction notes

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