Pyridine → 4-[(Chloromethyl)sulfanyl]pyridine

HRID 1196864

Reaction equation

HRID 1196864 reaction equation
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=1.[Cl:9]N1C(=O)CCC1=O.N1C=CC=CC=1>C1C=CC=CC=1>[Cl:9][CH2:1][S:2][C:3]1[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=1

Participants

5

Procedure

A solution of 4-methylthiopyridine (2.28 g, 18.2 mmol), N-chlorosuccinimide (3.0 g, 23 mmol) and pyridine (2.9 mL, 3.0 mmol) in benzene (40 mL) was heated at 50°-60° C. for 3 h. The mixture was allowed to cool to room temperature. The solvent was decanted and the residue was rinsed with benzene (2×10 mL). The organic phases were combined and evaporated. The residue was passed through a pad of silica gel (40 g) to give the title material (1.35 g) contaminated with the starting material. The impure product was repurified on silica gel preparative plates (eluted with CH2Cl2 /CH3CN: 1/1) to give the pure title material (926 mg, 32%) as a yellow oil.

Workup

  1. customThe solvent was decanted
  2. washthe residue was rinsed with benzene (2×10 mL)
  3. customevaporated

Sources & evidence

ORD record
ord-abb8f79711af4e5884a112e7965ac866
Source dataset
uspto-grants-1992_05
Patent number
US05116833

Linked notes

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