HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117789Generated: October 31, 2026
Methanol → 3-Bromo-6-methoxy-2-methylpyridine
https://huagongshe.com/reaction/2117789
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3,6-Dibromo-2-methylpyridine | HCID 2762946 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 3-Bromo-6-methoxy-2-methylpyridine | HCID 10798146 | 96% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442792B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-1d1e2c94392a45a48b1376369b5418e9 |
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| Source note | uspto-grants-2008_10 |
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