Carbon Tetrachloride → 2,4-Dichloro-5-(trichloromethyl)pyridine

HRID 2110148Notes

Reaction equation

HRID 2110148 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[CH:4][C:3]=1CO.S(Cl)(Cl)(=O)=O.[C:16]([Cl:20])(Cl)([Cl:18])[Cl:17]>>[Cl:8][C:6]1[CH:7]=[C:2]([Cl:1])[C:3]([C:16]([Cl:20])([Cl:18])[Cl:17])=[CH:4][N:5]=1

Participants

4

Procedure

To a solution of (4,6-dichloropyridin-3-yl)methanol (7 g, 39 mmol) in CCl4 (200 mL), was added sulfuryl dichloride (120 mL) dropwise with stirring. The resulting solution was heated at reflux overnight. The mixture was concentrated and the pH was adjusted to pH 8 by the addition of NaHCO3 (2N). The resulting solution was extracted with EtOAc (2×100 mL) and the organic layers were combined and dried over Na2SO4. The residue was purified by silica gel column chromatography to afford 1.2 g (12%) of 2,4-dichloro-5-(trichloromethyl)pyridine.

Workup

  1. temperatureThe resulting solution was heated
  2. temperatureat reflux overnight
  3. concentrationThe mixture was concentrated
  4. additionthe pH was adjusted to pH 8 by the addition of NaHCO3 (2N)
  5. extractionThe resulting solution was extracted with EtOAc (2×100 mL)
  6. dry with materialdried over Na2SO4
  7. customThe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-33d55977a3d74572abb044a77cbb6471
Source dataset
uspto-grants-2009_04
Patent number
US07517884B2

Reaction notes

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