Phosphorus oxychloride → HCID 178426119, compound

HRID 1501217Notes

Reaction equation

HRID 1501217 reaction equation
[OH:1][C:2]1[N:9]=[C:8]([CH3:10])[CH:7]=[C:6](O)[C:3]=1[C:4]#[N:5].P(Cl)(Cl)([Cl:14])=O>C(#N)C.[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1>[Cl:14][C:6]1[C:3]([C:4]#[N:5])=[C:2]([OH:1])[N:9]=[C:8]([CH3:10])[CH:7]=1

Participants

5

Conditions

Temperature
40 °C

Procedure

To a solution of 2,4-dihydroxy-6-methylnicotinonitrile (1.5 g, 10 mmol) in acetonitrile (50 mL) were added benzyltriethylammonium chloride (9.1 g, 40 mmol) and phosphoryl chloride (6.13 g, 40 mmol). The reaction mixture was heated to 40° C. for 4 hours at the same temperature. LC-MS showed that 2,4-dihydroxy-6-methylnicotinonitrile was consumed completely. The solvent was removed by rotary evaporation. To the residue was added dichloromethane (100 mL) and water (50 mL). The organic phase was separated, and it was washed with brine (50 mL) once, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give crude product, which was purified by silica gel column chromatography with dichloromethane/methanol=10:1 to afford 4-chloro-2-hydroxy-6-methylnicotinonitrile (800 mg, 24%) as a brown solid.

Workup

  1. customwas consumed completely
  2. customThe solvent was removed by rotary evaporation
  3. additionTo the residue was added dichloromethane (100 mL) and water (50 mL)
  4. customThe organic phase was separated
  5. washit was washed with brine (50 mL) once
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customto give crude product, which
  10. customwas purified by silica gel column chromatography with dichloromethane/methanol=10:1

Sources & evidence

ORD record
ord-02a158d436c24385b3966b60ac804c97
Source dataset
uspto-grants-2015_12
Patent number
US09206128B2

Reaction notes

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