Water → 2-Bromo-6-methylpyridin-3-ol

HRID 63264

Reaction equation

HRID 63264 reaction equation
[OH:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:8])=[N:6][CH:7]=1.[Br:9]Br.O>N1C=CC=CC=1>[Br:9][C:7]1[C:2]([OH:1])=[CH:3][CH:4]=[C:5]([CH3:8])[N:6]=1

Participants

5

Procedure

To a solution of 5-hydroxy-2-methylpyridine (Commercial, Aldrich, 44.5 g) in pyridine (400 ml) is added dropwise over 30 min at room temperature a solution of bromine (71.64 g) in pyridine (550 ml). The reaction mixture was stirred for an additional 1.5 h. The reaction mixture was poured into water (4 liters), stirred for a few minutes and extracted with diethyl ether (4×300 ml). The combined organics were dried over sodium sulphate and concentrated in vacuo to give a brown solid that was purified through silica using a 0-30% ethyl acetate in hexane system, to give the title compound as a beige solid, 37 g.

Workup

  1. stirringstirred for a few minutes
  2. extractionextracted with diethyl ether (4×300 ml)
  3. dry with materialThe combined organics were dried over sodium sulphate
  4. concentrationconcentrated in vacuo
  5. customto give a brown solid that
  6. customwas purified through silica using a 0-30% ethyl acetate in hexane system

Sources & evidence

ORD record
ord-f5e9f74c941d4f21b04a79c21b2e1bab
Source dataset
uspto-grants-2016_09
Patent number
US09447074B2

Linked notes

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