Phosphorus oxychloride → HCID 58009884, compound

HRID 2204517Notes

Reaction equation

HRID 2204517 reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]([C:11]([F:14])([F:13])[F:12])[C:5]([C:6]([NH2:8])=O)=[CH:4][N:3]=1.O=P(Cl)(Cl)Cl>>[Cl:1][C:2]1[CH:10]=[C:9]([C:11]([F:12])([F:13])[F:14])[C:5]([C:6]#[N:8])=[CH:4][N:3]=1

Participants

3

Conditions

Temperature
60 °C

Procedure

A mixture of 6-chloro-4-(trifluoromethyl)nicotinamide (0.847 g, 3.77 mmol, Preparation #27) and POCl3 (7.03 mL, 75.0 mmol) was heated at about 60° C. with stirring for about 1 h. The reaction mixture was cooled to ambient temperature and concentrated to dryness under reduced pressure and the resulting material was partitioned between chilled saturated aqueous NaHCO3 (30 mL) and EtOAc (30 mL). The layers were separated and the organic solution was washed with saturated aqueous NaHCO3 solution (30 mL) and brine (30 mL), dried over anhydrous Na2SO4, filtered, and concentrated to dryness under reduced pressure to give 6-chloro-4-(trifluoromethyl)nicotinonitrile (0.67 g, 86%) as a brown liquid: LC/MS (Table 2, Method a) Rt=2.31 min: 1H NMR (CDCl3) δ 8.87 (s, 1H), 7.75 (s, 1H).

Workup

  1. temperatureThe reaction mixture was cooled to ambient temperature
  2. concentrationconcentrated to dryness under reduced pressure
  3. customthe resulting material was partitioned
  4. temperaturebetween chilled saturated aqueous NaHCO3 (30 mL) and EtOAc (30 mL)
  5. customThe layers were separated
  6. washthe organic solution was washed with saturated aqueous NaHCO3 solution (30 mL) and brine (30 mL)
  7. dry with materialdried over anhydrous Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated to dryness under reduced pressure

Sources & evidence

ORD record
ord-8bb699c9d798486eb449df2c78f9fa03
Source dataset
uspto-grants-2016_06
Patent number
US09365579B2

Reaction notes

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