Pyridine → 2,6-Dichloropyridine-3-carbonitrile

HRID 31828Notes

Reaction equation

HRID 31828 reaction equation
[Cl:1][C:2]1[C:7](NC(=O)C)=[CH:6][CH:5]=[C:4]([Cl:12])[N:3]=1.[N:13]1C=CC=C[CH:14]=1.FC(F)(F)C(OC(=O)C(F)(F)F)=O>ClCCl>[Cl:1][C:2]1[C:7]([C:14]#[N:13])=[CH:6][CH:5]=[C:4]([Cl:12])[N:3]=1

Participants

5

Procedure

To a mixture of 2,6-dichloro-3-acetamidopyridine (6.3 g, 55% pure) and pyridine (4.93 ml, 61 mmole) in dichloromethane (100 ml), trifluoroacetic anhydride (4.23 ml, 30 mmole) was added. The reaction mixture was stirred at room temperature overnight and concentrated under reduced pressure. The crude product was purified by flash chromatography, eluting with 85% hexane: 15% ethyl acetate to give a pale yellow product (1.77 g, 90%).

Workup

  1. additionwas added
  2. concentrationconcentrated under reduced pressure
  3. customThe crude product was purified by flash chromatography
  4. washeluting with 85% hexane

Sources & evidence

ORD record
ord-c67edb3d78f349c98442b881ba67f6db
Source dataset
uspto-grants-2008_09
Patent number
US07425557B2

Reaction notes

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