Thionyl Chloride → 2-Chloro-3-chloromethyl-pyridine

HRID 1524322Notes

Reaction equation

HRID 1524322 reaction equation
[Cl:1][C:2]1[C:7]([CH2:8]O)=[CH:6][CH:5]=[CH:4][N:3]=1.S(Cl)([Cl:12])=O>C(Cl)(Cl)Cl.CN(C=O)C>[Cl:1][C:2]1[C:7]([CH2:8][Cl:12])=[CH:6][CH:5]=[CH:4][N:3]=1

Participants

5

Procedure

To a solution of the compound (18.5 g) obtained in step 1 in a mixture of chloroform (95 mL) and DMF (0.63 mL) was added thionyl chloride (14.0 mL) at 0° C., and the mixture was stirred at room temperature for 4 hr. The reaction mixture was concentrated under reduced pressure, and the residue was poured into a mixture of water and ethyl acetate. The solution was neutralized with sodium hydrogen carbonate, and the resultant product was extracted with ethyl acetate. The organic layer was washed with brine, and concentrated to give 2-chloro-3-(chloromethyl)pyridine (20.5 g, 89%) as a white powder.

Workup

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additionthe residue was poured into a mixture of water and ethyl acetate
  3. extractionthe resultant product was extracted with ethyl acetate
  4. washThe organic layer was washed with brine
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-941d562de62d47d9a59141d90f283c74
Source dataset
uspto-grants-2015_07
Patent number
US09079907B2

Reaction notes

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