Dimethyl Disulfide → 2-Bromo-5-(methylthio)pyridine

HRID 1815109Notes

Reaction equation

HRID 1815109 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5](Br)=[CH:4][N:3]=1.[CH3:9][S:10]SC>CCOCC.C([Li])CCC>[CH3:9][S:10][C:5]1[CH:6]=[CH:7][C:2]([Br:1])=[N:3][CH:4]=1

Participants

5

Procedure

To a solution of 2,5-dibromopyridine (23.4 g, 0.099 mol) in ether (500 mL), n-butyl lithium (1.52 M in n-hexane, 68 mL, 0.10 mmol) was added dropwise at −78° C. and the mixture was stirred for 1 hour at the temperature. Dimethyldisulfide (9.8 mL, 0.11 mol) was added slowly at −78° C. and the mixture was stirred for 1 hour at that temperature and further 1 hour at 0° C. The mixture was quenched with aqueous 1 N hydrochloric acid (200 mL) and extracted with ether (100 mL×2), dried over magnesium sulfate (MgSO4), and concentrated in vacuo gave the title compound (18.9 g, 94%).

Workup

  1. stirringthe mixture was stirred for 1 hour at that temperature and further 1 hour at 0° C
  2. customThe mixture was quenched with aqueous 1 N hydrochloric acid (200 mL)
  3. extractionextracted with ether (100 mL×2)
  4. dry with materialdried over magnesium sulfate (MgSO4)
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-2f1358730def43ccbc04d8c5de0f5b89
Source dataset
uspto-grants-2005_04
Patent number
US06878726B2

Reaction notes

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