Methanol → 3-Bromo-6-methoxy-2-methylpyridine

HRID 2117789Notes

Reaction equation

HRID 2117789 reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[C:4]([CH3:9])[N:3]=1.[OH2:10].[CH3:11][O-].[Na+].CO>C1(C)C=CC=CC=1.C(OC)(C)(C)C>[CH3:11][O:10][C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[C:4]([CH3:9])[N:3]=1

Participants

7

Conditions

Temperature
70 °C

Procedure

A solution of 2,5-dibromo-6-picoline (30.6 kg, 122 mol, 1.00 eq) in toluene (154.2 kg) was dried by vacuum distillation at 40° C./75 mmHg to remove 105.7 kg of distillate to produce a solution containing 40 ppm water. This was mixed with 25 weight % sodium methoxide in methanol (124.1 kg, 574 mol, 4.71 eq) and the mixture was heated at 65-75° C. for 6 hours until reaction completion, (HPLC analysis indicated 1.6 area % starting material remained). The mixture was cooled to 5° C. and water (98 L) was charged to the mixture followed by t-butylmethylether (97 kg). The layers were separated and the organic phase washed twice with 5% brine (139 kg) and once with 20% brine (165 kg). The organic phase was clarified by filtration and 51 kg was removed by vacuum distillation at 40° C. to produce a 2-methoxy-5-bromo-6-picoline solution (58.4 kg) of 40.6 wt % purity (96% yield). Part of this was purified by distillation for the purposes of recording the 13C NMR spectrum: 13C NMR (400 MHz, CDCl3) δ 162.4, 154.4, 142.0, 111.8, 109.5, 53.6, 24.6.

Workup

  1. customto remove 105.7 kg of distillate
  2. customto produce a solution
  3. temperatureThe mixture was cooled to 5° C.
  4. customThe layers were separated
  5. washthe organic phase washed twice with 5% brine (139 kg) and once with 20% brine (165 kg)
  6. filtrationThe organic phase was clarified by filtration and 51 kg
  7. customwas removed by vacuum distillation at 40° C.

Sources & evidence

ORD record
ord-1d1e2c94392a45a48b1376369b5418e9
Source dataset
uspto-grants-2008_10
Patent number
US07442792B2

Reaction notes

Loading…