Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-Methoxypyridine | HCID 74201 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-2-methoxypyridine | HCID 2734895 | 86.4% |
Reaction Steps
To a suspension of 2-methoxypyridine (1-1) (3.96 kg; 36.3 mol), NaOAc (3.57 kg; 39.9 mol), and dichloromethane (22 L) was added a solution of bromine (2.06 L; 39.9 mol) in dichloromethane (2 L), maintaining the reaction temperature below 7° C. over 2-3 hours. The mixture was aged for 1 hour at 0-7° C. and stirred at room temperature overnight. The reaction mixture was filtered and rinsed with dichloromethane (about 5 L). The filtrate and washings were combined, washed with cold 2 M NaOH (22 L; pH should be below 8) maintaining the temperature below 10° C., and with cold water (11 L). The organic layer was separated and concentrated under reduced pressure to give a crude product 1-2 (6.65 kg). The crude product was purified by vacuum distillation to give pure 1-2 (5.90 kg, 86%). Known compound: G. Butora et al., JACS, 119, 7694-7701 (1997).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472403B2 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-533500df325447799f03ca0b5234b7ad |
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| Source note | uspto-grants-2002_10 |
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