Benzyl Bromide → 1-Benzyl-4-methylpyridin-1-ium bromide

HRID 1808276Notes

Reaction equation

HRID 1808276 reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([CH3:7])=[CH:3][CH:2]=1.[CH2:8]([Br:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>C1(C)C=CC=CC=1>[Br-:15].[CH2:8]([N+:1]1[CH:6]=[CH:5][C:4]([CH3:7])=[CH:3][CH:2]=1)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1

Participants

4

Procedure

To a solution of 4-picoline (9.3 g, 0.1 mol) in toluene (200 mL), benzyl bromide (34.2 g, 0.2 mol) was added dropwise at room temperature. After the addition, the mixture was heated to reflux for 5 hrs. The mixture was cooled to room temperature. The precipitate formed was collected by filtration, washed with toluene and dried under vacuum to give Compound 1 as white solid (21.4 g, 81%). It was used without further purification. The structure of Compound 1 is given below:

Workup

  1. additionAfter the addition
  2. temperaturethe mixture was heated
  3. temperatureto reflux for 5 hrs
  4. customThe precipitate formed
  5. filtrationwas collected by filtration
  6. washwashed with toluene
  7. customdried under vacuum

Sources & evidence

ORD record
ord-081cf58f2130467593165e331443c32f
Source dataset
uspto-grants-2013_01
Patent number
US08357801B2

Reaction notes

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